Centurion Sterile Weitlaner Retractor 3 x 4 Prong — Class II medical device recall Z-1766-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-05-21, distributed nationwide. Three is the potential for the retractors to puncture through the sterile packaging.
| Recall number | Z-1766-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2025-04-09 |
| Classified | 2025-05-15 |
| Reported by FDA | 2025-05-21 |
| Distributed | Nationwide (US) |
| Quantity | 840 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00653160287011, 10653160287018 |
| Lot numbers | 2020061990, 2020070990, 2020110490, 2020111090, 2021082590, 2021121490, 2022062890, 2022110190, 2022121990, 2023032290, 2023032390, 2023092590, 2024050790, 2024053090, 2024062490, 2024070190 |
Product
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
Reason for recall
Three is the potential for the retractors to puncture through the sterile packaging.
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-1766-2025. 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.