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Zimmer® Air Dermatome, Zimmer® Dermatome AN Handpiece Recall Due to Zimmer Bi...

# Major Recall Alert: Zimmer® Air Dermatome, Zimmer® Dermatome AN Handpiece Recalled Due to Cutting Depth Issues

Zimmer Biomet has issued a phased, serial-specific medical device recall for its Zimmer® Air Dermatome and Zimmer® Dermatome AN handpieces. This urgent recall comes after multiple complaints reported that the devices were cutting beyond the intended depth due to a *misaligned thickness control bar*. Five cases have been reported in Canada—the serial complaints include CMP-0960689, CMP-0969102, CMP-0973010, CMP-0984249, and CMP-0987024.

This issue affects all devices manufactured between **March 2023 and April 2025**, provided they have not undergone repair or preventive maintenance. If left unaddressed, this defect may lead to potentially adverse outcomes, particularly in the first few uses. The defect was officially identified on **June 18, 2025**, through the company’s rigorous complaint handling process.

Learn about the risks and safety measures you need to take below.

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## Why This Recall is Important

The Zimmer® Air Dermatome and Zimmer® Dermatome AN handpieces are essential medical tools designed for precise skin grafting procedures, often used in surgical and burn recovery settings. A malfunction in these devices puts patients at significant risk, as improper cutting depth can lead to:

- **Unintended skin damage**: Risk of excessive tissue removal.
- **Compromised surgical outcomes**: Increased recovery time and complications.
- **Potential impact on patient safety** during critical medical treatments.

With **five complaints already reported in Canada**, this recall aims to prevent further incidents by removing affected units from clinical use.

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### Details of the Recall

Here’s everything you need to know about the Zimmer® Air Dermatome and Zimmer® Dermatome AN recall:

- **Affected Products**:
- Zimmer® Air Dermatome
- Zimmer® Dermatome AN Handpiece

- **Reason for Recall**: A defect in the thickness control bar leads to improper cutting depth, potentially causing adverse outcomes during use.

- **Complaints Reported in Canada**:
- CMP-0960689
- CMP-0969102
- CMP-0973010
- CMP-0984249
- CMP-0987024

- **Manufacturing Timeline**: All devices manufactured between **March 2023 and April 2025** that have not been serviced or repaired are affected.

- **Discovery Date**: The defect was confirmed on **June 18, 2025**, through complaint inspections.

For more information, visit the official recall notice: [Recalls and Safety Alerts | Government of Canada](https://recalls-rappels.canada.ca/en/alert-recall/zimmerr-air-dermatome-and-zimmerr-dermatome-handpieces).

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### What You Should Do

If your facility utilizes the Zimmer® Air Dermatome or Zimmer® Dermatome AN handpiece, follow these steps immediately:

1. **Check Manufacturing Dates**: Review all affected devices to confirm if they fall within the **March 2023 – April 2025** manufacturing range.

2. **Inspect Devices**: If you suspect a misaligned thickness control bar, cease use of the device immediately.

3. **Contact Zimmer Biomet**: Reach out to Zimmer Biomet for guidance on inspection, repair, or replacement.

4. **Report Adverse Incidents**: If your facility has experienced adverse effects linked to these devices, file a report with your governing health organization and update your clinical records.

5. **Share the Information**: Ensure your surgical team, supply chain department, and other stakeholders are informed of this recall.

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### Stay Safe – Get Instant Recall Alerts

Medical device recalls are a serious matter, and acting quickly can prevent harmful outcomes. Stay informed about the latest recalls by downloading our recall app. With instant notifications, easy search functionality, and up-to-date safety alerts, our app ensures you’ll never miss critical updates on medical device recalls.

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Ensure the safety of your patients and medical team—stay informed, stay alert, and act promptly.

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For detailed information on this recall, visit the official source here: [Recalls and Safety Alerts | Government of Canada](https://recalls-rappels.canada.ca/en/alert-recall/zimmerr-air-dermatome-and-zimmerr-dermatome-handpieces).

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