Carefusion recalls insulated bipolar forceps with missing instructions for power supply and cleaning. Owners should check model and lot numbers to determine if affected.
BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface with the device power supply, as well as cleaning and maintenance instructions. Refer to the attached V. Mueller" Bipolar Forcep IFU.
Carefusion is recalling insulated bipolar forceps that lack critical instructions for power supply and cleaning. This could lead to improper use if owners don't follow the missing safety steps.
The missing instructions could cause improper power supply connections or inadequate cleaning, potentially leading to equipment damage or infection risks. However, the hazard is not described as causing immediate injury.
Medical professionals using these forceps for surgery or procedures are most at risk. Owners of the specific model with UDI/DI 10885403040795 are affected.
Check for the model name: Carefusion V. Mueller"GERALD BIPOLAR FORCEPS INSULATED, 1.0MM TIP OVERALL LENGTH 7" (180MM), REF F-1112. Affected units have UDI/DI 10885403040795 across all lots.
Verify the product model and UDI/DI number to confirm if it matches the recalled item.
The recall is due to missing instructions for power supply and cleaning that could lead to improper use.
No, the recall does not require immediate discontinuation. Affected users should check the model and lot numbers.
Check the model and UDI/DI number to confirm if it's affected; no specific action is required beyond verification.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0382-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0382-2023 from Carefusion. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
