Carefusion 2200 Inc: Medical Device Recall in 2022 - (Recall #: Z-0401-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5016

Product Classification:

Class II

Date Initiated: November 2, 2022

Date Posted: December 14, 2022

Recall Number: Z-0401-2023

Event ID: 90967

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 25 units

Code Information:

UDI/DI 10885403041051, ALL LOTS

Distribution Pattern:

Nationwide, Austria, Canada, Egypt, Germany, Hong Kong, Israel, Philippines, Saudi Arabia, South Africa, South Korea, Thailand

Voluntary or Mandated:

Voluntary: Firm initiated