Health product recall

Zimmer Dermatome Blades

Last updated

Summary

Product
Zimmer Dermatome Blades
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Zimmer Dermatome Blades

65630969
65925347
65935738
65709066
65988623
65972711
65599469
65648460
65952858
65952857

00-8800-000-10

Issue

Zimmer Biomet Canada is initiating a lot specific recall for the Zimmer dermatome blades (00-8800-000-10) in Canada. There have been 38 complaints received related to skin grafts being thin and non-uniform when using the affected blades. The issue would be identified at the time of use and may result in the need for additional harvests to adequately cover the area. The trade-off of incomplete coverage versus having additional grafts is at the discretion of the health care provider based on the condition of the graft, overall patient condition, and severity of

the need for the graft.

The investigation identified an assignable cause within the manufacturing process, which was present for a defined amount 

Recall start date: September 12, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General and plastic surgery
Companies
Zimmer Surgical, Inc.
200 W. Ohio Avenue, Dover, Ohio, United States, 44622
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74309

Get notified

Receive notifications for new and updated recalls and alerts by category.

Subscribe