Recalls in Florida (page 6)
4115 recalls.
- Zoladex recall (TerSera Therapeutics LLC)
DrugClass IIReported October 7, 2026 · Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours. - Estradiol Gel recall (Amneal Pharmaceuticals, LLC)
DrugClass IIReported October 7, 2026 · Defective Container; packets were found to be either empty or partially full. - Ranolazine Extended-Release Tablets recall (Ajanta Pharma USA Inc)
DrugClass IIReported October 7, 2026 · Failed Dissolution Specifications: below specification - Atellica CH Revised C-Reactive Protein recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported October 7, 2026 · The potential for falsely elevated results. - HOPKINS Telescope 30¿ recall (Karl Storz Endoscopy)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect inside packaging label for eyepiece. - 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... - Olympus Tripp-Lite P580-025 25ft DisplayPort Cable recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported October 7, 2026 · While in the high-power operating mode, a video dropout/blackout may occur when using a particular accessory cable. - Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code:... recall (Micro Therapeutics, Inc.)
Medical deviceClass IIReported October 7, 2026 · Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter. - Evolution upgrade 1.5T amd Evolution upgrade 3.0T recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Upgrade to MR 7700 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Upgrade dStream recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - SmartPath to MR 7700 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - SmartPath to dStream for 1.5T recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - MR 7700 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - MR 5300 recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia Elition S and Ingenia Elition X. recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia Ambition S and Ingenia Ambition X. recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia 3.0T and 3.0T CX recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia 1.5T recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - Ingenia Blue Seal SE and Blue Seal XE recall (Philips North America)
Medical deviceClass IIReported October 7, 2026 · When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion... - NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I. recall (NOXBOX LTD)
Medical deviceClass IIReported October 7, 2026 · Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors. - 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... - PALACOS MV pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - PALACOS MV+G pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - PALACOS R+G pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - PALACOS R pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported October 7, 2026 · Potential for monomer liquid leakage. - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported October 7, 2026 · The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece... - 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... - Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v recall (Volcano Corp)
Medical deviceClass IIReported October 7, 2026 · Software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment. - 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) ... - Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED recall (Medline Industries, LP)
Medical deviceClass IReported October 7, 2026 · Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially... - Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories recall (Medline Industries, LP)
Medical deviceClass IReported October 7, 2026 · Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially... - Brand Name: Ferndale Laboratories recall (Custom Interventional Pain Management, LLC)
Medical deviceClass IIReported October 7, 2026 · Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits. - Agrish Reannounces and Expands Recall of Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Additional Units Added
Consumer productReported October 1, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped... - Golden Resale Recalls Portable Camping Showers Due to Risk of Serious Injury or Death from Fire Hazard
Consumer productReported October 1, 2026 · The recalled camping showers' immersion heaters can quickly ignite when they are partially or completely out of water, posing a risk of serious injury or death... - Dollar Tree Stores Recalls Electric Balloon Pumps Due to Burn Hazard
Consumer productReported October 1, 2026 · The recalled electric balloon pumps can overheat, posing a burn hazard. - Kobayashi Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported October 1, 2026 · The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn... - Walmart Recalls Over 4.4 Million Expert Grill Brushes Due to Ingestion Hazard
Consumer productReported October 1, 2026 · Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that... - Gobi Heat Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported October 1, 2026 · The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn... - GBYMIUY Recalls Magnetic Stick Figure Toy Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 1, 2026 · The magnetic stick figure toy sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to... - Designs Direct Recalls Cupcakes and Cashmere Brand Three-Light Floor Lamps, Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported October 1, 2026 · When plugged in or switched on, the lamp cord or internal wiring can smoke, melt, spark, overheat or ignite, posing a risk of serious injury from fire and burn... - LLK Trading Recalls Mochi Malrang Mystery Dumpling Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 1, 2026 · The mystery dumpling toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a... - YunHeng Recalls LandTale Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
Consumer productReported October 1, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - Gazelle USA Recalls Urban Arrow Cargo Electric Bikes Due to Fall Hazard
Consumer productReported October 1, 2026 · The front bolt in the seat post clamping mechanism can break, causing the seat to become loose, posing a fall hazard. - ABC Trading Recalls Squishy Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
Consumer productReported October 1, 2026 · The squishy toys violate the mandatory safety standard for toys because the water beads inside the toys expand larger than permitted, posing a deadly ingestion... - Brand Name: VOLARA System Product Name: VOLARA recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 30, 2026 · Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate. Affected devices returned to firm and... - 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... - nGenuity Patient Monitor with Capnography recall (Criticare Technologies, Inc.)
Medical deviceClass IIReported September 30, 2026 · Complaint trend where "Checkline Error" alarm presents at device setup, rendering the CO2 monitoring function inoperable. May result in procedure delay. - ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The... recall (Becton, Dickinson and Company)
Medical deviceClass IIReported September 30, 2026 · Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables. - Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234 recall (Philips Ultrasound, LLC)
Medical deviceClass IIReported September 30, 2026 · Due to software issue with ultrasound system, doppler sample is displayed shallower than its actual measurement location, potentially causing inaccurate blood... - SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head recall (SEASPINE ORTHOPEDICS CORPORATION)
Medical deviceClass IIReported September 30, 2026 · The proximal thread depth of the spinal device is out of design specification. - REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post... recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported September 30, 2026 · Labeling; Oxygen Cylinders do not contain required medical gas labeling - REF:HF2PC9 HomeFill Oxygen System recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported September 30, 2026 · Labeling; Oxygen Cylinders do not contain required medical gas labeling - HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported September 30, 2026 · Labeling; Oxygen Cylinders do not contain required medical gas labeling - 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... - Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black... recall (GIAS FOOD INC.)
FoodClass IReported September 30, 2026 · Contamination with Listeria monocytogenes - So Delicious Dairy Free Salted Caramel Cluster Cashewmilk recall (WWF Operating Company)
FoodClass IIReported September 30, 2026 · Product may contain foreign material: small stones and other hard objects. - Clear Eyes Redness Relief recall (Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - Clear Eyes Redness Relief recall (Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - Exenatide Injection recall (Amneal Pharmaceuticals of New York, LLC)
DrugClass IIReported September 30, 2026 · Defective Delivery System: Possibility of no medication in the prefilled pen. - Olanzapine Tablets recall (Macleods Pharmaceuticals Limited)
DrugClass IIIReported September 30, 2026 · Failed Impurities/Degradation Specifications:Organic and unspecified impurities above specification. - AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% recall (Sterling Pharmaceutical Services LLC)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - Lubricant Eye Drops-Cameron Pharmaceuticals recall (Sterling Pharmaceutical Services LLC)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - Major LubriFresh P.M. Nighttime Ointment recall (Sterling Pharmaceutical Services LLC)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - TRP The Relief Products* Gentle Eyes Lubricant Eye Drops recall (Sterling Pharmaceutical Services LLC)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - Reliable-1 Laboratories Lubricating Tears recall (Sterling Pharmaceutical Services LLC)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - Walgreens Lubricant Eye Drops recall (Sterling Pharmaceutical Services LLC)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - Walgreens Lubricant Eye Drops recall (Sterling Pharmaceutical Services LLC)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - Reliable -1 Laboratories recall (Sterling Pharmaceutical Services LLC)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% recall (Sterling Pharmaceutical Services LLC)
DrugClass IIReported September 30, 2026 · Lack of Assurance of Sterility - Medline Convenience Kits: 1) ANTERIOR SPINE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 30, 2026 · The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present... - Medline Convenience Kits: 1) MAJOR NEURO VCH recall (Medline Industries, LP)
Medical deviceClass IIReported September 30, 2026 · The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present... - Medline Convenience Kits: 1) MFC CRANIOTOMY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 30, 2026 · The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present... - Medline Convenience Kits: 1) MAJOR PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 30, 2026 · The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present... - Medline Convenience Kits: 1) PEDS SINUS PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 30, 2026 · The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present... - 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... - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator. - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator. - New York Embroidery Studio Trinity Non-Surgical Isolation Gown recall (New York Embroidery Studio, Inc.)
Medical deviceClass IIReported September 30, 2026 · Gowns do not consistently meet the minimum liquid-barrier performance required. - Cardioroot Woven Collagen Coated Vascular Graft recall (INTERVASCULAR, SAS)
Medical deviceClass IIReported September 30, 2026 · Product failed to meet the specified acceptance criteria for Integral Water Permeability (IWP). - REF: 81-030415 Myocardial Probe Non-Pyrogenic recall (DeRoyal Industries Inc)
Medical deviceClass IIReported September 30, 2026 · Myocardial temperature probes contain an incorrect needle. Specifically, an 18mm needle was included instead of a 15mm needle. - Brand Name: Pearle Vision 1 day Product Name: recall (CooperVision, Inc.)
Medical deviceClass IIReported September 30, 2026 · A small number of lenses within the affected lot are of the incorrect power. - Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model/Catalog Number: CD-B622LA. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive. - Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model/Catalog Number: CD-B620LA. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive. - Olympus BiCOAG Hemostasis Probe 10Fr Fixed Pin Connector. Model/Catalog Number: CD-B612LA. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive. - Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD-B610LA. recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 30, 2026 · Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive. - SmartPath to dStream for 1.5T recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction... - MR 7700 and Upgrade to MR 7700 recall (Philips North America Llc)
Medical deviceClass IIReported September 30, 2026 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction...