replacement available Recalls

1,215 recalls tagged with “replacement available”.

Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 9,500 IV Administration Sets for Backflow and Occlusion Risk (2025 Recall)

B. Braun Medical Inc. recalled 9,500 IV administration sets with worldwide distribution including the United States, Canada, Germany, Guatemala and Singapore. The devices may backflow medication from secondary piggyback IV containers into primary IV containers and may fail to prime. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer's recall’s,[

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall 2025 for Backflow and Occlusion Risk (490437)

B. Braun Medical recalled 4,536 IV administration sets globally after reports of backflow risk and occlusion. The sets labeled catalog 490437 are used with gravity IV administration and pump systems such as Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Patients and healthcare providers should stop using the devices immediately and follow the recall instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall 36,936 Units for Backflow and Occlusion Risk (2025)

B Braun Medical Inc. recalls 36,936 IV administration sets used with Infusomat Space and other pumps worldwide. The recall was announced Oct. 29, 2025 and includes US and international distribution to Canada, Germany, Guatemala and Singapore. The devices may allow backflow of medication from secondary containers into the primary container and cannot be primed. Stop using immediately and follow the

B Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recalled for Backflow Risk in 65,904 Units (2025)

B. Braun Medical recalled 65,904 IV Administration Sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The recall cites backflow of medication from secondary (piggyback) IV containers into primary containers and an inability to prime. Hospitals should stop using the devices immediately and follow the manufacturer's recall instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall for 1,250 Units Over Backflow Risk (2025)

B. Braun Medical recalled 1,250 IV administration sets distributed worldwide to hospitals and clinics. The devices may allow backflow of medication from secondary (piggyback) IV containers into primary containers and may not prime properly. Hospitals and other healthcare providers should stop using the devices immediately and follow recall instructions.

B. Braun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Vista IV Set Recall for 74,652 Units Over Backflow and Occlusion Risk

B Braun Medical Inc recalls 74,652 Vista IV sets used with Infusomat Space and Vista Basic Pumps due to backflow and occlusion risks. The recall affects devices distributed worldwide, including the US, Canada, Germany, Guatemala, and Singapore. Stop using the device immediately and follow manufacturer instructions.

BBraun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Illumina NextSeq 550Dx Reagent Kits Recalled for Leaky Flow Cells Affecting 11,916 Units Worldwide

Illumina recalled 11,916 NextSeq 550Dx reagent kits and flow cells worldwide after identifying a gasket defect that can leak during sequencing. The issue may cause run failures, no or insufficient data output, instrument fluidics clogs and potential exposure to toxic substances. Healthcare providers and users should stop using the affected kits and await recall instructions from Illumina.

Illumina
An instrument
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Food & Beverages
HIGH
FDA FOOD

Twin Sisters Creamery Whatcom Farmhouse Cheese Recalled for Potential Contamination (411 lbs, 2025)

Twin Sisters Creamery recalled 411 pounds of Whatcom Farmhouse cheese sold through Whole Foods Market after testing flagged potential STEC and E. coli O103 contamination. The recall is Class I. Consumers who bought this product should not eat it and should contact WFM Purchasing, LP for refund or replacement information.

Twin Sisters Creamery
Twin Sisters
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Food & Beverages
HIGH
FDA FOOD

Twin Sisters Creamery Whatcom Blue Sliced Cheese Recalled for STEC/E. coli Contamination (2025)

Twin Sisters Creamery recalled 411 pounds of Whatcom Blue Sliced Cheese sold by Whole Foods Market through distributor Peterson Company in Washington and Oregon. WSDA testing identified potential STEC and E. coli O103 contamination. Consumers who bought the cheese should not eat it and should contact WFM Purchasing, LP for a refund or replacement.

Twin Sisters Creamery
Twin Sisters
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Food & Beverages
HIGH
FDA FOOD

Water Pure My Bladder Recall for E. coli Contamination — 17,612 Bottles (2025)

Water Pure is recalling 17,612 bottles of My Bladder dietary supplement sold nationwide after an FDA notice cited possible contamination with E. coli O7:K1 and E. coli 1303. The contamination could cause illness. Consumers should not consume the product and should contact Water Pure for refund or replacement information.

Water Pure
Product may
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Recalled Bealife 5-Drawer Dresser (front)
HIGH
CPSC

Bealife 5-Drawer Dressers Recalled for Tip-Over Hazard in 2025

Bealife recalled its 5-Drawer Dressers on Oct. 23, 2025. The dressers are white and measure 32 inches high, 28 inches wide, and 16 inches deep. The model AP23-W is printed on packaging but not on the dresser itself. Consumers should stop using unanchored dressers and seek a full refund.

Bealife
The recalled
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Recalled Lifepro Sauna Blanket
HIGH
CPSC

Lifepro Bioremedy Infrared Sauna Blankets Recalled for Burn Hazard (2025)

Lifepro Fitness recalls Bioremedy Infrared Sauna Blankets sold with gray-faced controllers due to burn risk. The recall affects models LP-BRMDYL-BLK, LP-BRMDYL-GRY, LP-BRMDYR-BLK, LP-BRMDYR-GRY, LP-BRMDYR-BLU, LP-BRMDYR-PNK, and LP-BRMDYR-PRPL. Consumers should stop using and unplug the blankets and visit Lifepro’s recall page for a replacement.

Lifepro Fitness
The sauna
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Recalled Pack-N-Stroll Premium Folding Utility Wagon
HIGH
CPSC

Olympia Tools Recalls Pack-N-Stroll Premium Folding Utility Wagon for 2025 Entrapment and Falls Risk

Olympia Tools International recalls Pack-N-Stroll Premium Folding Utility Wagons sold at Costco after authorities determined the product can trap a child’s head and cause serious injury or death. The defect is an opening between the organizational tray and the sidewall. The wagon also lacks a restraint system. Stop using the wagon now and return it to Costco for a full refund.

Olympia Tools International
The utility
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Recalled Cranach Hardware Plastic Tip Restraint Kit
HIGH
CPSC

Cranach Hardware Recalls Tip Restraint Kits for Tip-Over Hazard (2025)

No injuries have been reported. Cranach Hardware recalled tip restraint kits sold through retailers after testing showed the plastic brackets and tie can fail to meet safety standards. Stop using the restraints and contact Cranach Hardware for a free stainless steel replacement kit.

Cranach Hardware
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed CareLink Clinic Recall 12,126 Units Worldwide in 2025

Medtronic MiniMed recalled 12,126 CareLink Clinic units worldwide after a software error misdisplays the 24-hour Sensor Glucose Overview Graph. The faulty software could prompt clinicians and patients to make therapy decisions based on incorrect glucose data. Patients should stop using the device immediately and contact Medtronic MiniMed or their healthcare provider for instructions.

Medtronic MiniMed
Software error
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Tag Statistics

Total Recalls
1,215

Related Tags

immediate actionstop use immediatelyfda regulatedcpsc regulatedinfant productadult productelectronicmetalplasticreturn for refundelectrical hazardchemical hazard