Recalls in Arkansas (page 23)
3931 recalls.
- Brand Name: B. BRAUN MEDICAL INC. Product Name: BPSK recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY ... recall (B Braun Medical Inc)
Medical deviceClass IIReported June 10, 2026 · B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall... - COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code:... recall (Covidien LLC)
Medical deviceClass IIReported June 10, 2026 · Due to customer complaint regarding incorrect display box labeling. - LVP software of the Ivenix Infusion System recall (Fresenius Kabi USA, LLC)
Medical deviceClass IReported June 10, 2026 · Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut... - Pediatric care bed recall (KAYSERBETTEN GMBH & CO. KG)
Medical deviceClass IReported June 10, 2026 · If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended... - Vornado Air Recalls SRTH Small Room Tower Heaters Due to Fire Hazard
Consumer productReported June 5, 2026 · The recalled heater's fan blade can detach from the motor shaft, which can cause the fan to slow or stop, leading to overheating and melting of the enclosure... - SUNS International Recalls Residential Elevator Interlock Switches Due to Fall and Crushing Hazard; Risk of Death or Serious Injury
Consumer productReported June 5, 2026 · The affected interlock switches can become stuck in a retracted position, allowing the exterior door to remain unlocked, posing a risk of death or serious... - TOMY Recalls Boon NURSH 8 oz Reusable Baby Bottles Due to Choking Hazard; Sold at Walmart
Consumer productReported June 5, 2026 · The hard plastic outer shell can bubble or partially peel off, resulting in loose pieces of film-like plastic that pose a choking hazard to young children. - Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Broqixin
Consumer productReported June 5, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and... - Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by Gudook Outdoor Sports
Consumer productReported June 5, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation and certification... - Crenlux Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Eicong
Consumer productReported June 5, 2026 · The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and... - Tiny Land Children's Play Tents Recalled Due to Risk of Injury from Irritation to Skin and Eyes
Consumer productReported June 5, 2026 · The recalled tents' fiberglass poles can shed fibers, posing an injury risk of skin and eye irritation. - Little Grape Land Recalls Nursing Pillows Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions
Consumer productReported June 5, 2026 · The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows and infant support... - Wyze Labs Recalls Solar Cam Pan Security Cameras Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported June 5, 2026 · The recalled Wyze Solar Cam Pan security cameras' incorrect assembly instructions can lead consumers to accidentally puncture the lithium ion battery's metal... - Fly By Jing recall (Fly By Jing Inc.)
FoodClass IIReported June 3, 2026 · Possible cross-contamination resulting in undeclared allergen ingredient (Peanut) - PRED MILD recall (AbbVie Inc.)
DrugClass IIIReported June 3, 2026 · Failed Stability Specifications - Nicotine Transdermal System Patch recall (AVEVA Drug Delivery Systems, Inc.)
DrugClass IIIReported June 3, 2026 · Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of... - Medline medical convenience kit labeled as EYE TRAY-LF recall (Medline Industries, LP)
Medical deviceClass IIReported June 3, 2026 · Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because... - Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 3, 2026 · It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of... - Azurion system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 3, 2026 · It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of... - Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation recall (Medtronic Neuromodulation)
Medical deviceClass IIReported June 3, 2026 · A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. - Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation recall (Medtronic Neuromodulation)
Medical deviceClass IIReported June 3, 2026 · A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates. - HydroMARK Breast Biopsy Site Marker recall (Devicor Medical Products Inc)
Medical deviceClass IIReported June 3, 2026 · Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers. - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection recall (Medline Industries, LP)
Medical deviceClass IReported June 3, 2026 · Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues... - Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 recall (O&M HALYARD INC)
Medical deviceClass IIReported June 3, 2026 · Nitrile Exam Glove failed to meet specifications chemical permeation performance. - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported June 3, 2026 · A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware updates... - Walmart Recalls Mainstays 9-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported May 28, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or... - Luminous Fidget Spinner Balls Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Anzmtosn
Consumer productReported May 28, 2026 · The recalled toys violate the mandatory safety standard for toys because the mini flashlight included with the fidget spinner balls contains button cell... - Missry Associates Recalls Misco Sports Light-Up Racket Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported May 28, 2026 · The racket sets violate the mandatory standard for toys because the screw on the racket used to secure the battery compartment does not remain attached when... - Joy Furniture Recalls Talan and Royce Living Room Furniture Sets Due to Risk of Serious Injury from a Fire Hazard
Consumer productReported May 28, 2026 · The power switch on the sofa, loveseat, or recliner can malfunction and overheat posing a risk of serious injury from a fire hazard. - Giantex Recalls Lounge Chairs Due to Amputation Hazard
Consumer productReported May 28, 2026 · Consumers can place their fingers in a pinch point, when adjusting the lounge chair, posing an amputation risk. - Tzumi Electronics Recalls SLF Sauna Blankets Due to Fire and Burn Hazards
Consumer productReported May 28, 2026 · The recalled sauna blankets can overheat, posing fire and burn hazards. - Lithium Coin Batteries Recalled Due to Battery Ingestion; Violates Federal Statute for Child-Resistant Packaging of Coin Batteries; Imported by Proudly American Store, of Canada
Consumer productReported May 28, 2026 · The recalled coin batteries are not in child-resistant packaging and do not bear the warning labels required under Reese's Law. When button cell or coin... - Daoen Recalls Zen Magnetic Promotional Ball Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
Consumer productReported May 28, 2026 · The recalled magnetic balls violate the mandatory standard for toys because they are loose high-powered magnets, posing an ingestion hazard to children. When... - MiniWarGaming and Primal Horizon Disc Magnets Recalled Due to Risk of Serious Injury or Death from Ingestion; Violate Mandatory Standard for Magnets; Imported by MiniWarGaming
Consumer productReported May 28, 2026 · The magnets violate the mandatory safety standard for magnets because the high-powered magnets fit within CPSC's small parts cylinder and are stronger than... - Giantex Recalls Giantex and Costway Portable Steam Saunas Due to Burn Hazard
Consumer productReported May 28, 2026 · The sauna's steam diffuser can be positioned too close to a consumer's body, allowing hot steam to come in contact with user, posing a burn hazard. - Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 ... recall (C.R. Bard Inc)
Medical deviceClass IIReported May 27, 2026 · Due to stain present on the surface of affected foley catheters. - Oncology Kit w/60" recall (ICU Medical, Inc.)
Medical deviceClass IIReported May 27, 2026 · Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak... - Swan-Ganz Pacing Catheter recall (Becton, Dickinson and Company)
Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection... - Swan-Ganz Jr Catheter recall (Becton, Dickinson and Company)
Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection... - Swan-Ganz Catheter recall (Becton, Dickinson and Company)
Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection... - Fisher Tex Mex Trail Mix 30 oz plastic jar recall (JOHN B SANFILIPPO & SONS INC)
FoodClass IReported May 27, 2026 · potential presence of Salmonella - Good & Gather Mexican Street Corn Trail Mix 8 oz bag recall (JOHN B SANFILIPPO & SONS INC)
FoodClass IReported May 27, 2026 · potential presence of Salmonella - Squirrel Brand Town & Country Mix 16 oz can recall (JOHN B SANFILIPPO & SONS INC)
FoodClass IReported May 27, 2026 · potential presence of Salmonella - Squirrel Brand Travelers Mix 16 oz can recall (JOHN B SANFILIPPO & SONS INC)
FoodClass IReported May 27, 2026 · potential presence of Salmonella - Southern Style Nuts Hunter Mix 30 oz plastic jar recall (JOHN B SANFILIPPO & SONS INC)
FoodClass IReported May 27, 2026 · potential presence of Salmonella - Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar recall (JOHN B SANFILIPPO & SONS INC)
FoodClass IReported May 27, 2026 · potential presence of Salmonella - Non Fat Dry Milk 1# recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - PSW21585 Save A Lot Bind 50# recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - Blackstone Parmesan Ranch Seasoning recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - 1P Jalapeno Heat Unit for 300 lbs of Meat recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - 1P Original Smokehouse Unit for 300 lbs. of Meat recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - Ellsworth Sour Cream + Onion Seasoning recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Prenatal+Postnatal Liquid Multivitamin Drops - Iron Free. Dosage: 3mL... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dosage: 3ml Liquid.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Kids Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Collagen Booster. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Women's Liquid Multivitamin Drops with Iron. Dosage: 3mL Liquid. Packaging:... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Mens 50+ Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging:... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - FulviLife Complex. Dosage:2 tablespoons recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Joint Nourish. Dosage:2 tablespoons recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns. - MG217 Multi-Symptom Treatment Cream & Skin Protectant recall (Wisconsin Pharmacal Company)
DrugClass IReported May 27, 2026 · Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus. - fentaNYL Citrate recall (IntegraDose Compounding Services LLC)
DrugClass IIReported May 27, 2026 · Subpotent Drug - cimzia recall (UCB Biosciences Inc.)
DrugClass IIReported May 27, 2026 · Lack of Assurance of Sterility - Erythromycin Tablets recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported May 27, 2026 · CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit - Erythromycin Tablets recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported May 27, 2026 · CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit - Estradiol Gel recall (ANI Pharmaceuticals, Inc.)
DrugClass IIReported May 27, 2026 · Defective Container; packets were found to be either empty or partially full. - Gas-X recall (Haleon US Holdings LLC)
DrugClass IIReported May 27, 2026 · Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling. - Liraglutide Injection recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported May 27, 2026 · Presence of particulate matter: a white thread-like structure in the cartridge - Busulfan Injection recall (Sagent Pharmaceuticals)
DrugClass IIIReported May 27, 2026 · Failed Impurities/Degradation Specifications - Primidone Tablets recall (Amerisource Health Services LLC)
DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. - Primidone Tablets recall (Amerisource Health Services LLC)
DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. - Primidone Tablets recall (Golden State Medical Supply Inc.)
DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. - Primidone Tablets recall (Golden State Medical Supply Inc.)
DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. - Primidone Tablets USP recall (Lannett Company Inc.)
DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. - Integris-Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 27, 2026 · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in... - Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 27, 2026 · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in... - Azurion system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 27, 2026 · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in... - Philips Azurion systems not configured with an optional auxiliary pan handle. Includes... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 27, 2026 · Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float... - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach.