Health product recall

V. Mueller Bipolar Forceps

Brand(s)
Last updated

Summary

Product
V. Mueller Bipolar Forceps
Issue
Medical devices - Labelling and packaging
What to do

Check for affected units, place/ maintain supplied IFU at appropriate location, share with users, return form. 

 

Audience
Healthcare
Industry

Affected products

Affected products

Lot or serial number

Model or catalogue number

V. Mueller Bipolar Forceps

All lots.

F-1335
F-1000
F-1003

V. Mueller Bipolar Forceps

All lots.

F-1300
F-2004
F-3010
F-1335
F-3015
F-1002
F-1030
F-5128
F-1000
F-3007
F-1003

Issue

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.

Recall start date: November 2, 2022

Additional information

Details
Original published date: 2022-11-18
Alert / recall type
Health product recall
Category
Health product - Medical device - General and plastic surgery
Companies

Carefusion

75 North Fairway Drive, Vernon Hills, Illinois, United States, 60061

Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Identification number
RA-72191