plastic Recalls

273 recalls tagged with “plastic”.

Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Blood Administration Set Recall 2025 for 24,624 Units Worldwide

B Braun Medical recalled 24,624 Blood Administration Sets worldwide. The recall covers sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The risk involves backflow from secondary IV containers into primary containers and the inability to prime. Hospitals and clinics should stop using the devices immediately and follow recall instructions.

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

B Braun Medical IV Administration Set Recall for 4,488 Units in 2025

B Braun Medical recalled 4,488 IV administration sets distributed worldwide, including the United States, Canada, Germany, Guatemala and Singapore. The devices risk backflow from secondary (piggyback) IV containers into primary containers and may be unable to prime due to occlusion. Healthcare facilities and patients should stop using immediately and follow recall instructions from the maker.

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

B. Braun Medical IV Administration Set Recall 122,232 Units Over Backflow Risk (2025)

B. Braun Medical recalled 122,232 IV administration sets sold worldwide through multiple medical distributors. The devices have a backflow risk from secondary (piggyback) IV containers into primary IV containers and may fail to prime. Hospitals and clinics should stop using the sets and follow the manufacturer's recall instructions.

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

B. Braun Medical IV Administration Set Recall for 5,952 Units Over Backflow Risk (2025)

B. Braun Medical Inc. recalled 5,952 IV Administration Sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore, for use with Infusomat Space, Outlook, and Vista Basic Pumps. The units carry Catalog Number 490612. The recall cites potential backflow from secondary piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare teams

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

B Braun Medical IV Administration Set Recall Affects 41,976 Units Worldwide (2025)

B Braun Medical recalled 41,976 IV Administration Sets sold worldwide after identifying a backflow risk. The device can allow medication to flow from secondary (piggyback) containers into the primary IV line and may not prime properly. Hospitals and healthcare providers should stop using the sets immediately and await recall instructions from B Braun Medical.

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

B. Braun Medical Recalls 7,008 IV Administration Sets for Infusomat Space Pumps (2025)

B. Braun Medical recalls 7,008 IV administration sets sold worldwide, including the United States, Canada, Germany, Guatemala and Singapore. The devices may backflow from secondary to primary IV containers and may fail to prime. Hospitals and patients should stop using the sets and follow the manufacturer’s recall instructions.

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

B Braun Medical IV Administration Set Recall 11,832 Units Over Backflow Risk (2025)

B Braun Medical recalled 11,832 IV administration sets worldwide on Oct 29, 2025. The devices are used with Infusomat Space, Outlook, and Vista Basic Pumps. The hazard is backflow of medication and occlusion. Stop using the product immediately and follow manufacturer recall instructions. Check your model numbers and contact the manufacturer for refunds or replacements.

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

B. Braun Medical IV Administration Set 490245 Recalled for Backflow Risk (2025)

B. Braun Medical Inc. recalls 40,992 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps sold to hospitals worldwide. The recall targets the IV administration set catalog number 490245. The defect is backflow of medication from secondary piggyback containers into primary containers and an inability to prime. Healthcare providers and patients should stop using theDevice

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

B. Braun Medical SAFELINE IV Sets Recalled for 46,250 Units Over Backflow Risk (2025)

B. Braun Medical recalled 46,250 SAFELINE IV sets sold worldwide on Oct. 29, 2025. The devices pose a backflow risk from secondary piggyback IV containers into primary lines and may fail to prime due to occlusion. Hospitals and patients using Infusomat Space Large Volume Pump, Outlook Pump, or Vista Basic Pump with SAFELINE sets should stop use immediately and await manufacturer instructions.

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

B. Braun Medical IV Administration Set Recall Affects 286,400 Units Across Global Pumps (2025)

B. Braun Medical recalls 286,400 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump worldwide. The devices may backflow from secondary IV containers into primary containers and cannot be primed. Stop using the device immediately and follow recall instructions from the manufacturer.

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

B. Braun Medical Anesthesia IV Set Recalled for Backflow Risk (10,536 Units) 2025

B. Braun Medical recalled 10,536 Anesthesia IV Sets sold through multiple retailers worldwide after a potential backflow from piggyback to primary IV lines and occlusion. The devices are used with Infusomat Space Large Volume Pumps, Outlook Pumps, and Vista Basic Pumps. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

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

B. Braun Medical Recalled 19,320 Anesthesia IV Sets for Backflow Risk (2025)

B. Braun Medical Inc. recalled 19,320 Anesthesia IV Sets used with Infusomat Space Large Volume Pumps and related BBMI devices sold worldwide through healthcare facilities. The devices pose a backflow risk from secondary piggyback IV containers into the primary IV container and cannot be primed. Healthcare facilities and patients should stop using the device immediately and follow the manufacturer

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

B. Braun Medical 490238 Extension Set Recalled for IV Backflow Risk (2025)

B. Braun Medical's 490238 Extension Set, used with Infusomat Space Large Volume Pumps and other BBMI devices, is recalled worldwide to hospitals and clinics. The device can allow backflow from secondary piggyback IV containers into the primary container and cannot be primed. Healthcare facilities should stop using the device immediately and follow the manufacturer's recall instructions.

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

B. Braun Medical Blood Administration Set Recall 7,344 Units Over Backflow Risk (2025)

B. Braun Medical recalled 7,344 Blood Administration Sets used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The devices may allow backflow from secondary (piggyback) IV containers into primary IV containers and cannot be primed. Hospitals and healthcare providers should stop using the devices immediately and follow manufacturer instructions.

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

BBraun Medical Blood Administration Set Recall 5,448 Units (2025)

BBraun Medical recalled 5,448 Blood Administration Sets used with Infusomat Space pumps worldwide sold to hospitals. The recall cites potential backflow of medication from secondary piggyback IV containers into primary IV containers and an inability to prime. Healthcare facilities should stop using the sets immediately and follow recall instructions from B. Braun Medical.

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

B Braun Medical IV Administration Sets Recalled for Backflow Risk and Occlusion (2025)

B Braun Medical Inc. recalls 111,312 IV Administration Sets worldwide, including US and international markets, due to backflow risk and occlusion. The recall affects catalog numbers 490193 and 490326, used with Infusomat Space, Outlook, and Vista Basic pumps. Stop using immediately and follow recall instructions for refunds or replacements.

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

BBMIs Infusomat IV Administration Set Recall, 63,192 Units Worldwide for Backflow and Occlusion Risk

BBMI recalled 63,192 IV administration sets worldwide on Oct 29, 2025. The recall affects the IV administration set labeled as 490426 with UDIs listed. The defect is potential backflow from secondary to primary IV containers and an inability to prime. Patients and healthcare providers should stop using these devices immediately and follow the manufacturer’s recall instructions.

BB Braun Medical
Potential for
Read more
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
Read more
Previous
12345...14
Next

Tag Statistics

Total Recalls
273

Related Tags

back to schoolimmediate actionstop use immediatelyreturn for refundreplacement availableinfant productadult productworkplacemetalelectronicbathroomkitchen
    plastic Recalls | RecallRadar