Medical device recalls (page 6)
2545 recalls.
- 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... - Halyard IV START KIT NON-STERILE REF: KRIV26-02 recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides - 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. - DuoGlide Short-Term Straight Dialysis Catheter recall (Bard Access Systems, Inc.)
Medical deviceClass IReported September 23, 2026 · this is a downstream recall of class I recall RES 98777 - Power-Trialysis Short-Term Straight Dialysis Catheter recall (Bard Access Systems, Inc.)
Medical deviceClass IReported September 23, 2026 · this is a downstream recall of class I recall RES 98777 - AMS Convenience Kit: DSAEK Pack - RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported September 16, 2026 · The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that... - Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - MedicaLyte Bicarbonate Powder REF: DB+201-2.1 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - HeartSine SAM 350P 350P US Device recall (HeartSine Technologies Ltd)
Medical deviceClass IIReported September 16, 2026 · Due to a damaged (over stretched) membrane tail that causes an intermittent fault. - Products that contain the Pericare Wipes: recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF:... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: *Bardex¿ I.C. Complete Care¿ Foley Catheter... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray ... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser... recall (Lutronic Corporation)
Medical deviceClass IIReported September 16, 2026 · Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in... - Halyard IV Start Kit Non-Sterile REF: KRIV26-02 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 16, 2026 · Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper... - Kit: Single Shot Epidural 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IReported September 16, 2026 · Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. - Kit: Epidural/Pain TQC 20/Cs recall (Medical Action Industries, Inc. 306)
Medical deviceClass IReported September 16, 2026 · Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. - Bravo CF capsule delivery device recall (Given Imaging Ltd.)
Medical deviceClass IReported September 16, 2026 · Capsule may fail to attach to the esophagus or detach from the delivery device. Risks include patient aspiration/inhalation, perforation of esophagus... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Citrasate recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - NaturaLyte recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - GRANUFLO Dry Acid Concentrate: Product Numbers: 0FD2251-3B recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog... recall (B Braun Medical Inc)
Medical deviceClass IIReported September 9, 2026 · Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label. - Velys Enabling Tech Robotic-Assist Station REF: 451611001 recall (Medos International Sarl)
Medical deviceClass IIReported September 9, 2026 · Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning. - 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... - LUX-Dx recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 9, 2026 · There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed... - LUX-Dx recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 9, 2026 · There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed... - LUX-Dx recall (Boston Scientific Corporation)
Medical deviceClass IIReported September 9, 2026 · There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed... - 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... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - HEALON EndoCoat PRO recall (Johnson & Johnson Surgical Vision, Inc.)
Medical deviceClass IIReported September 9, 2026 · Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered... - Medline Convenience Kits: 1) BLOOD DRAW KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ORTHO ASPIRATION KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) EYE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) C-SECTION PREP recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) LABOR CDS recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) PRE-OP KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IV START KIT LAB DRAW-SH recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ARTERIAL LINE INSERTION KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IV START KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ULTRASOUND BREAST PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) COLORECTAL ME recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IVS BLOOD CULTURE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) DYKM1414 recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) CDS840396X recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - STA Staclot Protein S recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported September 9, 2026 · A positive drift in QC values within the reagent's stated 4-hour onboard stability period was identified - Halyard medical convenience kits labeled as: 1) A-P PACK - 205936 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - 1) NEURO recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - Halyard medical convenience kits labeled as: 1) ENT recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231 recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Philips Ingenuity CT Product Codes: Ingenuity CT Upgrades 728327 recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Philips IQon Spectral CT Product Codes: IQon Spectral CT 728332 recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - Philips Brilliance. Models: Brilliance iCT recall (Philips North America Llc)
Medical deviceClass IIReported September 9, 2026 · Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of... - FRU recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 2, 2026 · Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults... - PORTRAIT CORE SERVICES SOFTWARE V1.0.5 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 2, 2026 · Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults... - PORTRAIT COMPUTE AND CORE SERVICES V1.2 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 2, 2026 · Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults... - PORTRAIT CORE SERVICES SOFTWARE V1.1 recall (GE Medical Systems Information Technologies Inc)
Medical deviceClass IIReported September 2, 2026 · Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults... - POWERSEAL 5 MM recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 2, 2026 · Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. - ORT300 recall (IMRIS Imaging Inc)
Medical deviceClass IIReported September 2, 2026 · The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and... - ORT200 recall (IMRIS Imaging Inc)
Medical deviceClass IIReported September 2, 2026 · The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and... - healthmark ProChek-W Protein Test for Robotic Arms recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - healthmark ProChek-II recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - FUJIFILM Synapse PACS software v7.4.310 recall (FUJIFILM Healthcare Americas Corporation)
Medical deviceClass IIReported September 2, 2026 · Software issue may cause the ruler measurement to be inaccurate.