# FDA recall Z-1440-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-02-23.

## Product

Centurion Clamp kits labeled as:   a) STERILE BACKHAUS TOWEL CLAMP (BTC173), Product Code 66520;   b) STERILE TOWEL CLAMP, Product Code A547ST;   c) ST TOWEL CLAMPS NON PERFORATING (P/S), Product Code I68080;   d) STERILE TOWEL CLAMPS 5 1/2, Product Code I68085;   e) STERILE TOWEL CLAMPS 5 1/2", Product Code I68095;   f) ZIPSER PENIS CLAMP STERILE (ZC110), Product Code ZC110ST

## Reason for recall

Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

## Distribution

Worldwide distribution - US Nationwide and the countries of Panama, Canada.

## Key facts

- **Recall number:** Z-1440-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-23
- **Report date:** 2024-04-10

- **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-1440-2024

## Citation

> AI Analytics. FDA recall Z-1440-2024. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-1440-2024. Source: US FDA. Licensed CC0.

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