# FDA recall Z-0133-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-09-03.

## Product

(1) Centurion Sterile CirClamp, Reorder #200CR;  (2) Centurion CirClamp with 1.1cm Bell and Insert, Reorder #210CR, Sterile;  (3) Centurion CirClamp with 1.13cm Bell and Insert, Reorder #230CR, Sterile;  (4) Centurion CirClamp with 1.45cm Bell and Insert, Reorder #245CR, Sterile;  (5) Centurion CirClamp with 1.1cm Bell, Reorder #310CR, Sterile;  (6) Centurion CirClamp with 1.1cm Bell Reprocessed, Reorder #310CRK, Sterile;  (7) Centurion CirClamp with 1.3cm Bell, Reorder #330CR, Sterile;  (8) Centurion CirClamp with 1.3cm Bell Reprocessed, Reorder #330CRK, Sterile;  (9) Centurion CirClamp with 1.6cm Bell, Reorder #345CR, Sterile;  (10) Centurion CirClamp with 1.45cm Bell, Reorder #3145CR, Sterile;  (11) Centurion CirClamp with 1.1cm Bell & Insert Reprocessed, Reorder #CR210K, Sterile;  (12) Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile;  (13) Centurion CirClamp with 1.145cm Bell & Insert Reprocessed, Reorder #CR245K, Sterile;  (14) Centurion CirClamp 

## Reason for recall

Product has been identified as having holes in the packaging.

## Distribution

Worldwide distribution - US Nationwide and the countries of India and Panama.

## Key facts

- **Recall number:** Z-0133-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-09-03
- **Report date:** 2024-10-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0133-2025

## Citation

> AI Analytics. FDA recall Z-0133-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0133-2025. Source: US FDA. Licensed CC0.

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