(1) Centurion Sterile CirClamp, Reorder #200CR; (2) Centurion… — Class II medical device recall Z-0133-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-10-30, distributed nationwide. Product has been identified as having holes in the packaging.
| Recall number | Z-0133-2025 |
|---|---|
| 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 | 2024-09-03 |
| Classified | 2024-10-18 |
| Reported by FDA | 2024-10-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | IN, PA |
| Quantity | 498,354 kits |
| UPC / GTIN / UDI-DI | 00653160197440, 00653160197457, 00653160197464, 00653160197471, 00653160197488, 00653160197495, 00653160197501, 00653160309898, 00653160309904, 00653160312898, 00653160312904, 00653160312935, 00653160312942, 00653160312959, 10653160197447, 10653160197454, 10653160197461, 10653160197478, 10653160197485, 10653160197492, 10653160197508, 10653160278139, 10653160309895, 10653160309901, 10653160312895 and 4 more |
| Lot numbers | 2021092490, 2021092990, 2021100190, 2021100590, 2021101190, 2021102590, 2021102690, 2021102890, 2021110590, 2021110890, 2021111890, 2021112990, 2021120690, 2021120990, 2021121390, 2021121590, 2021121690, 2021122090, 2021122190, 2021122790, 2022010590, 2022011090, 2022012090, 2022012490, 2022020390, 2022021890, 2022022101, 2022022190, 2022022201, 2022022490, 2022022801, 2022030101, 2022030290, 2022030301, 2022030401, 2022030701, 2022030790, 2022031490, 2022031601, 2022031701 and 205 more |
Product
(1) Centurion Sterile CirClamp, Reorder #200CR; (2) Centurion CirClamp with 1.1cm Bell and Insert, Reorder #210CR, Sterile; (3) Centurion CirClamp with 1.13cm Bell and Insert, Reorder #230CR, Sterile; (4) Centurion CirClamp with 1.45cm Bell and Insert, Reorder #245CR, Sterile; (5) Centurion CirClamp with 1.1cm Bell, Reorder #310CR, Sterile; (6) Centurion CirClamp with 1.1cm Bell Reprocessed, Reorder #310CRK, Sterile; (7) Centurion CirClamp with 1.3cm Bell, Reorder #330CR, Sterile; (8) Centurion CirClamp with 1.3cm Bell Reprocessed, Reorder #330CRK, Sterile; (9) Centurion CirClamp with 1.6cm Bell, Reorder #345CR, Sterile; (10) Centurion CirClamp with 1.45cm Bell, Reorder #3145CR, Sterile; (11) Centurion CirClamp with 1.1cm Bell & Insert Reprocessed, Reorder #CR210K, Sterile; (12) Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile; (13) Centurion CirClamp with 1.145cm Bell & Insert Reprocessed, Reorder #CR245K, Sterile; (14) Centurion CirClamp with 1.6cm Bell Reprocessed, Reorder #CR345K, Sterile; and (15) Centurion Sterile CirClamp with 1.45cm Bell Reprocessed, Reorder #CR3145K.
Reason for recall
Product has been identified as having holes in the 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-0133-2025. 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.