medical MODERATE Updated 2023-04-26

MEDLINE INDUSTRIES, LP - Northfield recalls Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reo

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Recalled Product

Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile.

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Hazard / Issue

The CirClamp subassembly found in the kit was the incorrect size.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #2022070590, Exp. 2026-08-31, UDI (01)10653160312895(10)2022070590(17)260831.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

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