BBraun Medical Recalls

7 recalls found for BBraun Medical. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

BBraun Medical Inc. Recalled 104,784 Anesthesia IV Sets Over Backflow, Occlusion Risk

BBraun Medical Inc. recalled 104,784 Anesthesia IV Sets used with Infusomat Space, Outlook, and Vista Basic pumps. The recall cites backflow of medication from secondary to primary IV containers and a potential inability to prime. Health care providers should stop using the devices immediately and follow the manufacturer’s recall instructions for refund or replacement.

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

B Braun Medical IV Set Recall Affects 32,436 Units Over Backflow and Occlusion Risks (2025)

B Braun Medical Inc. recalled 32,436 Anesthesia IV Sets used with Infusomat Space, Outlook Pump, and Vista Basic Pump after reports of backflow risk and occlusion. The recall covers catalog numbers 490189 and 490226 distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. Consumers should stop using the device immediately and follow manufacturer instructions for recall. A

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

B Braun Medical Inc. Recalls 28,344 IV Administration Sets Linked to Backflow and Occlusion Risks (Z

B Braun Medical Inc. recalls 28,344 IV administration sets used with several BBMI infusion pumps after reports of backflow and occlusion risks. The recall covers a catalog number 470179 device distributed worldwide including the U.S., Canada, Germany, Guatemala and Singapore. The issue involves potential backflow from secondary IV containers into primary containers and the inability to prime the管.

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

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

B Braun Medical Inc recalled 1,019 IV administration sets worldwide after reports of backflow and occlusion. The devices were used with BBMI Infusomat Space, Outlook, and Vista Basic pumps. The recall affects a single catalog number 457506 with UDI details. Patients should stop using the device and follow manufacturer instructions for return.

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

B Braun Medical IV Administration Sets Recall Over Backflow and Occlusion Risk (2025)

B Braun Medical Inc. recalls 190,625 IV administration sets worldwide, including US and Canada, for risk of backflow from secondary to primary IV containers and occlusion that prevents priming. The recall affects BBMI’s Infusomat Space, Outlook Pump, and Vista Basic Pump compatible sets. Stop-use immediately and follow recall instructions.

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

BBraun Medical IV Administration Set Recalled for Backflow and Occlusion Risk (490491, 2025)

BBraun Medical Inc recalls 960 IV administration sets distributed worldwide due to backflow risk and inability to prime. The recall affects the IV administration set catalog number 490491 with UDI-DI 04046955086931. The device can allow medication to flow from secondary piggyback containers into primary IV containers and may not prime properly. Stop using immediately and follow recall instructions

BBraun Medical
Potential for
Read more
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
Read more

Brand Statistics

Total Recalls
7
Pages
1

Related Brands

B Braun MedicalB Braun Medical Inc