FDA Device recall Z-1766-2025
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
- FDA Device
- Class II
- ongoing
- Published 2025-05-21
On 2025-05-21 the FDA classified a Class II recall of Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395 by Medline Industries Northfield, citing three is the potential for the retractors to puncture through the sterile packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1766-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-04-09 |
| Published | 2025-05-21 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
Reason
Three is the potential for the retractors to puncture through the sterile packaging.
Identifiers
| code_info | UDI/DI 10653160287018 (each) 00653160287011 (case), Lot Numbers: 2020061990, 2020070990, 2020110490, 2020111090, 20210…UDI/DI 10653160287018 (each) 00653160287011 (case), Lot Numbers: 2020061990, 2020070990, 2020110490, 2020111090, 2021082590, 2021121490, 2022062890, 2022110190, 2022121990, 2023032290, 2023032390, 2023092590, 2024050790, 2024053090, 2024062490, 2024070190. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1766-2025%22
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