No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
No image published for this recall
Zimmer® air dermatome and zimmer® dermatome an handpieces
Official notice
3 Dec 2025
An official Health Canada notice concerns Zimmer® air dermatome and zimmer® dermatome an handpieces. Zimmer Biomet is conducting a phased serial specific medical device recall for the Zimmer® Air Dermatome and Zimmer® Dermatome AN handpieces. Multiple complaints have been received related to dermatome devices that were cutting beyond the proper depth. Five complaints have been reported in Canada, they are CMP-0960689, CMP-0969102, CMP-0973010, CMP-0984249 and CMP-0987024. Inspections of the returned complaint devices confirmed that affected devices may have a misaligned thickness control bar. If the device has a misaligned thickness control bar from manufacture, it would be expected to manifest such that any potential negative outcomes would be present upon the first few uses. All devices manufactured between March 2023 and April 2025, that have not been returned for repair or preventive maintenance, are within scope of the recall. The defectiveness was discovered on June 18, 2025. Issue was identified through the complaints handling process. Published 2025-12-03.
What to do now
Contact the manufacturer if you require additional information.
Recall number
81318
Official notice
2025-12-03
The hazard
The hazard
Zimmer Biomet is conducting a phased serial specific medical device recall for the Zimmer® Air Dermatome and Zimmer® Dermatome AN handpieces. Multiple complaints have been received related to dermatome devices that were cutting beyond the proper depth. Five complaints have been reported in Canada, they are CMP-0960689, CMP-0969102, CMP-0973010, CMP-0984249 and CMP-0987024. Inspections of the returned complaint devices confirmed that affected devices may have a misaligned thickness control bar. If the device has a misaligned thickness control bar from manufacture, it would be expected to manifest such that any potential negative outcomes would be present upon the first few uses. All devices manufactured between March 2023 and April 2025, that have not been returned for repair or preventive maintenance, are within scope of the recall. The defectiveness was discovered on June 18, 2025. Issue was identified through the complaints handling process.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
Checked manually this time?
The app alerts you when a new official recall is published — no searching, no checking back.
Turn on recall alertsAffected products
Affected products
Product 1
Product 2
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Manufacturer
Phone
Brand: Zimmer Surgical Also Trading Relign, Zimmer® Air Dermatome And Zimmer® Dermatome An Handpieces.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
View full official noticeRelated recalls
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
A.t.s® 4000 ts tourniquet systems single and dual hose with cpc connectors
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
A.t.s.® 5000ts (tourniquet system) with hoses and lop sensor (personalized pressure)
Brand match
Medium risk
Markets
CriticalVevor 4 in 1 baby walker recalled
Brand match
Critical risk
Markets
HighCombined smoke, combustible gas & carbon monoxide alarm recalled
Brand match
High risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Omni-tract surgical retractor system
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Urinary catheter trays containing cliniclean pericare wipes
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Rapidlab® 348ex system
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Airseal access port with blunt obturator and airseal access port with optical obturator
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Wasplab
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Lifecodes lsa class ii
Brand match
Medium risk
Markets
No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
Nephromax high pressure nephrostomy balloon catheter
Brand match
Medium risk
Markets
CriticalIpex cement and primer products recalled
Brand match
Critical risk
Markets
Weekly recall digest
Get next week's recalls before you need them.
One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.
The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.
This recall was published 3 Dec 2025. The next one won't wait for you to search.
RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.