PlainRecalls
FDA Devices Moderate Class II Ongoing

CareFusion V. Mueller CUSHING MICRO BIPOLAR FORCEPS 0.7MM TIP, OVERALL LENGTH 6" (150MM), REF F-52000

Reported: December 14, 2022 Initiated: November 2, 2022 #Z-0417-2023

Product Description

CareFusion V. Mueller CUSHING MICRO BIPOLAR FORCEPS 0.7MM TIP, OVERALL LENGTH 6" (150MM), REF F-52000

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.

Details

Recalling Firm
Carefusion 2200 Inc
Units Affected
239 units
Distribution
Nationwide, Austria, Canada, Egypt, Germany, Hong Kong, Israel, Philippines, Saudi Arabia, South Africa, South Korea, Thailand
Location
Vernon Hills, IL

Frequently Asked Questions

What product was recalled?
CareFusion V. Mueller CUSHING MICRO BIPOLAR FORCEPS 0.7MM TIP, OVERALL LENGTH 6" (150MM), REF F-52000. Recalled by Carefusion 2200 Inc. Units affected: 239 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 14, 2022. Severity: Moderate. Recall number: Z-0417-2023.