Identity Shoulder System Resection Planer 35mm Resection Planer
Reported: February 15, 2023 Initiated: December 7, 2022 #Z-1098-2023
Product Description
Identity Shoulder System Resection Planer 35mm Resection Planer
Reason for Recall
Two planers were found to be unusable during sawbones shoulder training.
Details
- Recalling Firm
- Zimmer, Inc.
- Units Affected
- 84 units
- Distribution
- US Nationwide distribution in the states of AR, CA, IL, MI, NJ, NY, OK, PA, TX, and WA.
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
Identity Shoulder System Resection Planer 35mm Resection Planer. Recalled by Zimmer, Inc.. Units affected: 84 units.
Why was this product recalled? ▼
Two planers were found to be unusable during sawbones shoulder training.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 15, 2023. Severity: Moderate. Recall number: Z-1098-2023.
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