Carefusion recalls specific bipolar forceps due to missing instructions for power supply and cleaning. Owners should check model numbers and contact Carefusion for details.
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 a specific type of bipolar forceps because the instructions for use are incomplete. This could lead to improper cleaning or power supply issues if users follow outdated or missing guidelines.
The missing instructions could result in improper cleaning or incorrect power supply connections, potentially causing damage to the device or affecting surgical outcomes. However, the hazard does not involve immediate physical harm like injury or fire.
Medical professionals using these forceps in surgeries or procedures are most at risk. Owners of the specific model number are likely affected.
Check for the model number F-2004 on the forceps, which includes a 2.0mm tip and 7-1/2" (190mm) insulated length. The recall covers all lots of this specific product.
Look for the model number F-2004 on the forceps to confirm if it is recalled.
The recall is due to missing instructions for power supply and cleaning that are in the manufacturer's original instructions.
No, but you should check the model number to confirm if it is recalled. The recall does not require immediate discontinuation.
Contact Carefusion directly for details about the specific model and next steps.
We’ve drafted a message you can send Carefusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0391-2023 — Carefusion Carefusion Hello, I own a Carefusion that is covered by recall Z-0391-2023 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.
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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.
