Centurion CirClamp with 1 — Class II medical device recall Z-1407-2023
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2023-04-26, distributed nationwide. The CirClamp subassembly found in the kit was the incorrect size.
| Recall number | Z-1407-2023 |
|---|---|
| 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 | 2023-03-02 |
| Classified | 2023-04-19 |
| Reported by FDA | 2023-04-26 |
| Distributed | Nationwide (US) |
| Quantity | 162 units |
| UPC / GTIN / UDI-DI | 10653160312895 |
| Lot numbers | 2022070590 |
| Expiration dates | 2026-08-31 |
Product
Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile.
Reason for recall
The CirClamp subassembly found in the kit was the incorrect size.
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-1407-2023. 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.