Recall Z-1098-2023— Zimmer, Inc.
Class II · Ongoing
Class II FDA medical device recall by Zimmer, Inc., initiated 2022-12-07. FDA's recall record names no specific 510(k) clearance for this event. Product: Identity Shoulder System Resection Planer 35mm Resection Planer. Reason: Two planers were found to be unusable during sawbones shoulder training..
- Recalling firm
- Zimmer, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-12-07
- Firm location
- Warsaw, IN, United States
Product description
Identity Shoulder System Resection Planer 35mm Resection Planer
Reason for recall
Two planers were found to be unusable during sawbones shoulder training.
Data sourced from openFDA. This site is unofficial and independent of the FDA.