Zimmer Oscillating Flat — Class II medical device recall Z-0466-2016
Terminated recall by Synvasive Technology Inc, reported 2015-12-30, distributed in CA, CT, MA. Two lots of oscillating saw blades incorrectly identify the blade cutting width as 25mm instead of the correct
| Recall number | Z-0466-2016 |
|---|---|
| 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 | 2015-12-08 |
| Classified | 2015-12-22 |
| Reported by FDA | 2015-12-30 |
| Terminated | 2016-11-01 |
| Distributed | CA, CT, MA |
| Quantity | 14 |
| Lot numbers | 43054, 45104 |
| Model numbers | 11-4770, 19075127YT1 |
Product
Zimmer Oscillating Flat - TS ST Hub; 75mm x 19mm x 1.00/1.27mm; Synvasive Part No. 11-4770: Part No. 19075127YT1; Lot No. 45104 and 43054 Description: STRYK_76542K_19X75X1.27T General and Plastic Surgery: The oscillating surgical saw blade is intended for use with powered equipment to resect bone and/or cartilage in orthopedic procedures
Reason for recall
Two lots of oscillating saw blades incorrectly identify the blade cutting width as 25mm instead of the correct specification of 19mm.
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-0466-2016. 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.