adult product Recalls

989 recalls tagged with “adult product”.

Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Infusomat IV Sets Recalled for Backflow and Occlusion Risk (49,330,370 Units)

B. Braun Medical recalled 49,330,370 Infusomat IV sets worldwide after a potential backflow from secondary to primary IV containers and an inability to prime. The recall covers gravity IV sets and pump sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Stop using any affected sets immediately and contact B. Braun Medical for instructions on refunds or replacement

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 DRUG

Agebox iKids-Growth Recalled Over Undeclared Ibutamoren

Agebox recalled its iKids-Growth Night Formula due to the presence of undeclared ibutamoren. The recall affects 60-count bottles manufactured exclusively for AGEBOX Inc. Consumers should stop using the product immediately and contact Agebox or their healthcare provider for guidance.

Agebox
Marketed Without
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Health & Personal Care
HIGH
FDA DRUG

Agebox iKids-Growth Capsules Recalled Over Undeclared Ingredient

AGEBOX Inc. recalled 665 bottles of iKids-Growth capsules on October 28, 2025, due to undeclared ibutamoren. The product was marketed without an approved NDA/ANDA. Consumers should stop using the product immediately and contact Agebox for guidance.

Agebox
Marketed Without
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Adhesive Bandages Over Sterility Concerns

Medline Industries recalled 1.57 million units of Curad Touch-Free and Quick-Strip Bandages on October 27, 2025. The packaging may exhibit open seals, compromising sterility. Consumers should stop use immediately and follow the recall instructions provided by the manufacturer.

Medline Industries, LP
Medline has
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls CURAD Germ-Shield Bandages Over Sterility Risk

Medline Industries recalled 182,526 units of CURAD Germ-Shield Touch-Free Fabric Bandages due to compromised sterility. The recall affects all lots manufactured and distributed in the US, Guam, Canada, and the UAE. Consumers must stop using these bandages immediately.

Medline Industries, LP
Medline has
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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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Health & Personal Care
HIGH
FDA DRUG

Cipla USA Recalls Lanthanum Carbonate Tablets Over Stability Issues

Cipla USA recalled 1,180 boxes of Lanthanum Carbonate chewable tablets on October 24, 2025. The recall follows a failure to meet stability specifications for hardness tests. Consumers and healthcare providers must stop using the product immediately.

LANTHANUM CARBONATE
Failed stability
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Medical Solutions USA Recalls MAMMOMAT Inspiration Operator Table for Bus-Installation Risk

Siemens Medical Solutions USA recalls the MAMMOMAT Inspiration operator table. The recall covers six units worldwide, including three in the United States. The operator table was sold with a bus-installation kit and is not designed or released for bus installations. Stop using the device immediately and contact Siemens for instructions.

Siemens Medical Solutions USA
There were
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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 Sauna Model Tylö Halmstad 2
MEDIUM
CPSC

Sauna360 Recalls Tylö Halmstad and Kiruna Hybrid Saunas Over Fall Hazard

Sauna360 recalls Tylö Halmstad and Kiruna Hybrid saunas sold by Sauna360 distributors nationwide from July 2024 through December 2024 for between $6,000 and $12,000. The recall targets bench seating that can collapse, creating a fall hazard. Stop using the benches immediately and contact Sauna360 for a free repair.

Sauna360
The saunas
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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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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Due to Hazardous Events

Olympus Corporation of the Americas recalled the Thunderbeat, 5 mm, 45 cm, Pistol Grip device on October 22, 2025. The recall affects 30 units distributed worldwide, including the U.S., Canada, Brazil, Germany, Mexico, and Japan. Patients and healthcare providers must stop using this device immediately due to reports of adverse events.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Over Adverse Events

Olympus Corporation of the Americas recalled the Thunderbeat 5 mm, 35 cm, Front-Actuated Grip on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients must stop using this product immediately.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Over Adverse Events

Olympus Corporation of the Americas recalled the Thunderbeat surgical device on October 22, 2025, due to reports of adverse events. The recall affects 30 units distributed worldwide, including the US, Canada, and Japan. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Firm is
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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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Health & Personal Care
HIGH
FDA DRUG

Bristol-Myers Squibb Opdualag Vial Recall for Sterility Risk: 12,778 Units (2025)

Bristol-Myers Squibb recalled 12,778 Opdualag single-dose vials nationwide after a lack of assurance of sterility was identified. The product is nivolumab and relatlimab-rmbw injection. The recall date is 2025-10-21. Healthcare providers should stop using affected lots and follow the recall letter guidance.

Opdualag
Lack of
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Tag Statistics

Total Recalls
989

Related Tags

immediate actionstop use immediatelyreplacement availablereturn for refundelectrical hazardchemical hazardinfant producttoddler productchoking hazardfire hazardtip over risksuffocation risk