Lead recalls
349 recalls.
- Carevo recall (ARJOHUNTLEIGH POLSKA Sp. z.o.o.)
Medical deviceClass IIReported November 4, 2026 · The side support of the shower trolley may open unintentionally when the handles are not fully locked and additional force is applied during patient handling.... - Nalu TD2 Therapy Disc with firmware recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported November 4, 2026 · Therapy Disc (TD) that powers and sends stimulation signals to an Implantable Pulse Generator (IPG), part of a neurostimulation system, has a firmware issue... - OmniaSecure Model 3930M recall (Medtronic, Inc.)
Medical deviceClass IIReported November 4, 2026 · Affected leads require additional engineering evaluation due to complaints regarding difficulty in achieving fixation during implantation. Potential harm of... - Great Value Fruit Cocktail in Fruit Juice from Concentrate recall (Pacific Coast Producers)
FoodClass IIReported October 28, 2026 · Potential contamination with elevated levels of lead. - Sempio Yellow Peach recall (Sempio Food Services, Inc)
FoodClass IIReported October 28, 2026 · elevated level of lead in canned peaches - InterStim Percutaneous Extensions EXT 3560022 ISTM II PERC 3560022 EXT... recall (Medtronic Neuromodulation)
Medical deviceClass IIReported October 28, 2026 · Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the system from working as intended and may... - InterStim SureScan MRI Leads 978A1 & 978B1: LEAD 978A128 ISTM MICRO 28CM SSMRI... recall (Medtronic Neuromodulation)
Medical deviceClass IIReported October 28, 2026 · Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the system from working as intended and may... - TS Misc. Instruments Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Femoral Prep Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - TS Universal Baseplate Finishing Tray recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported October 21, 2026 · Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the... - LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762. recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIIReported October 21, 2026 · In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct... - MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control recall (Microgenics Corporation)
Medical deviceClass IIReported October 21, 2026 · Vial-to-vial variability in MAS¿ Omni"IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone... - Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 ... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported October 21, 2026 · Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift... - Power F2 Powered Fastening System recall (Ferno-Washington Inc)
Medical deviceClass IIReported October 21, 2026 · Firmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to the system... - BARD EP XT DECAPOLAR STEERABLE recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported October 14, 2026 · Diagnostic electrophysiology (EP) catheter may have a breached sterile barrier on the straight seal side of the primary pouch, which if used could lead to... - Battle Bandage recall (Safeguard US Operating LLC)
Medical deviceClass IIReported October 14, 2026 · Compression bandage may be degraded, which may cause unwanted foreign material to be introduced inside the wound, which may lead to wound exploration and... - Lior brand Cinnamon Ground Seasoning recall (Galil Importing Corp)
FoodClass IIReported October 7, 2026 · Product contains elevated levels of lead. - CHARLOTTE CLAW Screw recall (Wright Medical Technology, Inc.)
Medical deviceClass IIReported October 7, 2026 · Screws, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the screwheads... - Brand Name: Tandem t:slim mobile application Product Name: t:slim Mobile Application recall (Tandem Diabetes Care, Inc.)
Medical deviceClass IIReported October 7, 2026 · A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a software issue preventing successful pairing of the t:slim application... - Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported October 7, 2026 · Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the... - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary... recall (American Contract Systems Inc)
Medical deviceClass IIReported October 7, 2026 · Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the... - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary... recall (American Contract Systems Inc)
Medical deviceClass IIReported October 7, 2026 · Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the... - Medical convenience kits containing BD CliniClean Pericare Wipes within BD Urinary... recall (American Contract Systems Inc)
Medical deviceClass IIReported October 7, 2026 · Kits contain manufacturer-recalled perineal care (pericare) wipes within urinary catheter trays, which may be contaminated with a lubricant used during the... - Brand Name: Opportunity Pro Product Name: Opportunity Pro Model/Catalog Number: 72-50800 recall (American Nitrile Operations Llc)
Medical deviceClass IIReported October 7, 2026 · Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to... - Brand Name: Opportunity Flex Product Name: Opportunity Flex Model/Catalog Number:... recall (American Nitrile Operations Llc)
Medical deviceClass IIReported October 7, 2026 · Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to... - Brand Name: Performance Pro Product Name: Performance Pro Model/Catalog Number:... recall (American Nitrile Operations Llc)
Medical deviceClass IIReported October 7, 2026 · Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to... - EnCor EnCompass Breast Biopsy and Tissue Removal System Console recall (Bard Peripheral Vascular Inc)
Medical deviceClass IIReported October 7, 2026 · Breast biopsy and tissue removal system may experience the following errors: 1) Probe calibration and /or handheld driver failure (code HH01-00020009) , 2) ... - VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable... recall (Draeger, Inc.)
Medical deviceClass IReported October 7, 2026 · Potential cracks in the hose, which could lead to leakage or the hose falling off. - PRO+ 40" MRS SURFACE recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 30, 2026 · There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved... - PRO+ 36" MRS SURFACE recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 30, 2026 · There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved... - PRO+ MRS SURFACE FOR VERSACARE recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 30, 2026 · There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved... - Presource Convenience Kits: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 30, 2026 · The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could... - Presource Convenience Kits: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 30, 2026 · The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could... - VITEK 2 AST-N461 TEST KIT recall (Biomerieux Inc)
Medical deviceClass IIReported September 30, 2026 · The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe... - INCA recall (CooperSurgical, Inc.)
Medical deviceClass IReported September 30, 2026 · Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP... - INCA recall (CooperSurgical, Inc.)
Medical deviceClass IReported September 30, 2026 · Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP... - Convenience kits CATARACT PACK DYNJ59881A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A recall (Medline Industries, LP)
Medical deviceClass IIReported September 23, 2026 · Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to... - Blood Culture Collection Venipuncture Kit 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IIReported September 23, 2026 · Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may... - Brand Name: VERIQA recall (PTW FREIBURG)
Medical deviceClass IIReported September 23, 2026 · When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may... - Core Services Hub V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Workflow Core Services V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity PACS Server V7 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity PACS V2 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Enterprise Archive V8 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - Centricity Enterprise Archive V2 recall (GE Healthcare)
Medical deviceClass IIReported September 23, 2026 · Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs... - NOxBOXi Nitric Oxide Delivery System. recall (NOXBOX LTD)
Medical deviceClass IIReported September 23, 2026 · Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation. - Oncology sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Oncology sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - IV Non-Dedicated Gravity Administration Sets with drip chambers recall (ICU Medical, Inc.)
Medical deviceClass IIReported September 23, 2026 · Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl... - Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 23, 2026 · Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically... - Medline Convenience Kits: 1) DYNDB3086D recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) DYNDH1193 recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) DYKM1000B recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) ACC010308A recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) OPEN HEART ADULT recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET recall (Medline Industries, LP)
Medical deviceClass IReported September 23, 2026 · The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the... - BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump... recall (BD SWITZERLAND SARL)
Medical deviceClass IReported September 23, 2026 · Due to discrepancies in specific attributes in the performance data for infusion sets, which may lead to inappropriate pump performance. - SQT Recalls Lontcs Busy Boards Due to Risk of Serious Injury from Lead Poisoning; Violate Federal Lead Paint Ban
Consumer productReported September 10, 2026 · The toys’ zipper contains levels of lead that exceed the standard set in the federal lead paint ban. Lead is toxic if ingested by young children and can cause... - 5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ORTHO... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators CATARACT... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators C-SECTION... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators LABOR... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PATIENT... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators DELUXE... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - MONDRAKER USA Recalls Mountain Bicycles Equipped with ONOFF S9 Carbon MTB Handlebars Due to Risk of Serious Injury or Death from Fall Hazard
Consumer productReported September 3, 2026 · The affected handlebars may crack or fracture during use, which can lead to loss of control, posing a risk of serious injury or death from fall hazard. - Onli 17cm Hydrophilic Urethral Intermittent Catheter recall (Hollister Ulc)
Medical deviceClass IIReported September 2, 2026 · Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might... - Beckman Coulter recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported August 26, 2026 · Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine... - Syva EMIT 2000 Quinidine Assay REF: 4Q019UL Contents: 1x28 mL recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported August 26, 2026 · Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine... - Arrow-LOK Implant recall (Arrowhead DE LLC)
Medical deviceClass IIReported August 26, 2026 · Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection. - ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000 recall (Erbe USA Inc)
Medical deviceClass IIReported August 19, 2026 · A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in... - ProNephro AKI recall (Bioporto Diagnostics A/S)
Medical deviceClass IIReported August 19, 2026 · The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or... - Endo-Model recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported August 19, 2026 · The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a... - Philips Azurion recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 19, 2026 · Two software related issues: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate... - Philips Azurion Rystem recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported August 19, 2026 · Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural... - Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623 recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING ... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 ... recall (Covidien, LP)
Medical deviceClass IIReported August 19, 2026 · Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to... - 5-PLASMA Bivalirudin Control recall (Aniara Diagnostica LLC)
Medical deviceClass IIReported August 12, 2026 · Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of... - 5-PLASMA Bivalirudin Calibrator recall (Aniara Diagnostica LLC)
Medical deviceClass IIReported August 12, 2026 · Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of... - 5-PLASMA Bivalirudin AMR Verification Kit recall (Aniara Diagnostica LLC)
Medical deviceClass IIReported August 12, 2026 · Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of... - Atellica CH Urine Albumin REF: 11537225 recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported August 12, 2026 · Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely... - HardyDisk AST Cefiderocol 30¿g recall (Hardy Diagnostics)
Medical deviceClass IIReported August 12, 2026 · Due to incorrect cartridges include in affected products that there is the potential for false-susceptible or false-resistant susceptibility results and may...