ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1 — Class II medical device recall Z-1676-2020
Terminated recall by Synvasive Technology Inc, reported 2020-04-15, distributed in AL, NY. Mislabeled: Actual blade width is 19 mm but the label indicates a width of 25 mm.
| Recall number | Z-1676-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Synvasive Technology Inc, El Dorado Hills, CA, United States |
| Recall initiated | 2018-07-27 |
| Classified | 2020-04-06 |
| Reported by FDA | 2020-04-15 |
| Terminated | 2021-06-07 |
| Distributed | AL, NY |
| Quantity | 266 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00846795028320 |
Product
ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic procedures. Manufactured By: Synvasive Technology, Inc., a Subsidiary of Zimmer
Reason for recall
Mislabeled: Actual blade width is 19 mm but the label indicates a width of 25 mm.
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-1676-2020. 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.