Carefusion 2200 Inc 2022-12-14 Health serious FDA
Health · FDA · Recall #FDA-Z-0411-2023
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 0.5MM TIP, ANGLED-UP FINE OVERALL… Recall
Issued December 14, 2022 · Carefusion 2200 Inc
In December 2022, Carefusion 2200 Inc recalled the CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 0.5MM TIP, ANGLED-UP FINE OVERALL…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 0.5MM TIP, ANGLED-UP FINE OVERALL… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Carefusion 2200 Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Carefusion 2200 Inc
- Category
- Health
- Recall date
- December 14, 2022
- Units affected
- Not reported
- Sold at
- Nationwide, Austria, Canada, Egypt, Germany, Hong Kong, Israel, Philippines, Saudi Arabia, South Africa, South Korea, Thailand
- Recall number
- FDA-Z-0411-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Carefusion 2200 Inc has 8 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.