Medline recalls Centurion CirCl: 1.3cm Bell & Insert Reprocessed kits due to incorrect size subassembly. Affected units have specific lot/expiry codes. Stop using immediately.
The CirClamp subassembly found in the kit was the incorrect size.
Medline is recalling Centurion CirClamp kits with a 1.3cm Bell and Insert that contain an incorrect size subassembly. This could lead to improper use in medical procedures if the wrong size is installed.
The subassembly in the kit is the wrong size, which could cause improper function during medical procedures. This might lead to incorrect application or failure to secure the device properly.
Healthcare professionals using the Centurion CirClamp kits for medical procedures are most at risk. Patients receiving these kits during surgery could be affected if the incorrect size is used.
Check for lot number 2022070590 and expiration date 2026-08-31 on the kit. The product has a unique identifier starting with UDI (01)10653160312895(10)2022070590(17)260831.
Discard the Centurion CirClamp kit with the incorrect size subassembly to prevent potential improper use during medical procedures.
The CirClamp subassembly in the kit is the incorrect size, which could lead to improper function during medical procedures.
Stop using it immediately and discard the kit to prevent potential improper use during medical procedures.
Check for lot number 2022070590 and expiration date 2026-08-31 on the kit. The product has a unique identifier starting with UDI (01)10653160312895(10)2022070590(17)260831.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1407-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1407-2023 from Medline Industries. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
