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:
Alert / recall type
Health product recall
Category
Health products - Medical devices - 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
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