Centurion Clamp kits labeled as: a) STERILE BACKHAUS TOWEL CLAMP — Class II medical device recall Z-1440-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-04-10, distributed nationwide. Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The
| Recall number | Z-1440-2024 |
|---|---|
| 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 | 2024-02-23 |
| Classified | 2024-03-29 |
| Reported by FDA | 2024-04-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, PA |
| Quantity | 12,980 units |
| Reason classes | sterility, packaging |
| UPC / GTIN / UDI-DI | 00653160040968, 00653160113686, 00653160232608, 00653160232615, 00653160232691, 00653160258462, 10653160113683, 10653160258469, 20653160232602, 20653160232695, 30653160232616, 60653160040960 |
| Lot numbers | 2023020990, 2023022490, 2023032290, 2023033090, 2023041090, 2023052290, 2023060790, 2023062690, 2023062890, 2023071790, 2023072790, 2023092990, 2023111590 |
Product
Centurion Clamp kits labeled as: a) STERILE BACKHAUS TOWEL CLAMP (BTC173), Product Code 66520; b) STERILE TOWEL CLAMP, Product Code A547ST; c) ST TOWEL CLAMPS NON PERFORATING (P/S), Product Code I68080; d) STERILE TOWEL CLAMPS 5 1/2, Product Code I68085; e) STERILE TOWEL CLAMPS 5 1/2", Product Code I68095; f) ZIPSER PENIS CLAMP STERILE (ZC110), Product Code ZC110ST
Reason for recall
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
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-1440-2024. 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.