FDA Device recall Z-1407-2023
Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile
- FDA Device
- Class II
- ongoing
- Published 2023-04-26
On 2023-04-26 the FDA classified a Class II recall of Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile by Medline Industries Northfield, citing the CirClamp subassembly found in the kit was the incorrect size.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1407-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-02 |
| Published | 2023-04-26 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile.
Reason
The CirClamp subassembly found in the kit was the incorrect size.
Identifiers
| code_info | Lot #2022070590, Exp. 2026-08-31, UDI (01)10653160312895(10)2022070590(17)260831. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1407-2023%22
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