Identity Shoulder System Resection Planer 35mm Resection Planer — Class II medical device recall Z-1098-2023
Ongoing recall by Zimmer, Inc., reported 2023-02-15, distributed nationwide. Two planers were found to be unusable during sawbones shoulder training.
| Recall number | Z-1098-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2022-12-07 |
| Classified | 2023-02-06 |
| Reported by FDA | 2023-02-15 |
| Distributed | Nationwide (US) |
| Quantity | 84 units |
| UPC / GTIN / UDI-DI | 00889024628052, 00889024628069, 00889024628076, 00889024628083, 00889024628090 |
| Lot numbers | ZB7234013, ZB7234014, ZB7234015, ZB7252285, ZB7298335 |
Product
Identity Shoulder System Resection Planer 35mm Resection Planer
Reason for recall
Two planers were found to be unusable during sawbones shoulder training.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1098-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.