FDA Device recall Z-1676-2020
ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic procedures
- FDA Device
- Class II
- terminated
- Published 2020-04-15
On 2020-04-15 the FDA classified a Class II recall of ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for bone or cartilage in orthopedic procedures by Synvasive Technology, citing mislabeled: Actual blade width is 19 mm but the label indicates a width of 25 mm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1676-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-07-27 |
| Published | 2020-04-15 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Synvasive Technology |
| Distribution | AL, NY |
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
Mislabeled: Actual blade width is 19 mm but the label indicates a width of 25 mm.
Identifiers
| code_info | Lot Number/UDI: 265474 (01)00846795028320(17)220414(10)265474 304117 (01)00846795028320(17)230131(10)304117 317918 (01)00846795028320(17)230531(10)317918 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1676-2020%22
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