# FDA recall Z-1441-2024

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

## Product

Centurion manual surgical kits labeled as:   a) STERILE TUBE OCCLUDING FORCEP (TO8256), Product Code 66225;   b) ST. KELLY HEMO W/TIPS (SK8039), Product Code 66565;   c) STERILE BUTTERFLY PROBE (P837), Product Code 66810;   d) STERILE PROBE (PR5), Product Code 66900;   e) STERILE NAIL NIPPER, Product Code 67110;   f) STERILE FREER SEPTUM ELEVATOR (FE75B), Product Code 67285;   g) STERILE 5 1/2" NAIL NIPPER (32195), Product Code 67365;   h) STERILE 4 1/4" CUTICLE NIPPER (32908), Product Code 67420;   i) STERILE ENGLISH ANVIL NAIL SPLITTER-5", Product Code 67595;   j) STERILE UNIVERSAL RING CUTTER(FS02470), Product Code 67780;   k) STERILE FINGER NAIL CLIPPER, Product Code 589784ST;   l) BILLEAU EAR LOOP 4MM 6" LARGE, Product Code BEL46ST;   m) PROBE WITH EYE, Product Code DYND04011;   n) STERILE 9" MAYO SCISSOR (ST150), Product Code I67350;   o) STRL ROCHESTER OCHSNER SATIN 7 1/4", Product Code I67695;   p) CMP* NAIL NIPPER ANGLED 4.5, Product Code I67980;   q) STERILE BILLEAU EAR LOOP 

## 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-1441-2024
- **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-1441-2024

## Citation

> AI Analytics. FDA recall Z-1441-2024. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/Z-1441-2024. Source: US FDA. Licensed CC0.

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