Turbett Surgical Container — Class II medical device recall Z-1037-2023
Ongoing recall by Turbett Surgical, Inc., reported 2023-02-08, distributed nationwide. Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instruments leadin
| Recall number | Z-1037-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Turbett Surgical, Inc., Victor, NY, United States |
| Recall initiated | 2022-12-05 |
| Classified | 2023-01-30 |
| Reported by FDA | 2023-02-08 |
| Distributed | Nationwide (US) |
| Quantity | 61 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00859464007281 |
Product
Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
Reason for recall
Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instruments leading to infection or other major injuries.
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-1037-2023. 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.