# FDA recall Z-1437-2024

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

## Product

Centurion Forcep kits labeled as:  a) STERILE F/P SPLINTER FORCEP (SF6141), Product Code 66165;  b) STERILE WEBSTER NEEDLEHOLDER, Product Code 66185;  c) STERILE ADSON FORCEP SERR (598), Product Code 66195;  d) STERILE DRESSING FORCEP SERR (DF6003), Product Code 66200;  e) STERILE TISSUE FORCEP W/TEETH (TF6015), Product Code 66205;  f) STERILE F/P WEBSTER NEEDLEHOLDER FN8064, Product Code 66220;  g) STERILE IRIS FORCEP W/TEETH (IF250), Product Code 66275;  h) STERILE TUBE CLAMP (TOC500), Product Code 66280;  i) STERILE F/P SATIN NEEDLEHOLDER (FN9050S), Product Code 66355;  j) STERILE 9 1/2 SPONGE FORCEP (237), Product Code 66360;  k) STERILE SATIN NEEDLEHOLDER (FN6060S), Product Code 66375;  l) STERILE CURV CRILE FORCEP (CF81810), Product Code 66395;  m) STERILE LUCAE FORCEP (BF212), Product Code 66415;  n) STERILE 6" SF MAYO NEEDLEHOLDER P/S, Product Code 66430;  o) STERILE SATIN FORCEP W/TEETH (AF058S), Product Code 66440;  p) STERILE 6" FACIAL NEEDLEHOLDER (FN7070S), Product Code 66

## 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-1437-2024
- **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-1437-2024

## Citation

> AI Analytics. FDA recall Z-1437-2024. Retrieved 2026-08-13 from https://api.ai-analytics.org/recall/Z-1437-2024. Source: US FDA. Licensed CC0.

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