# FDA recall Z-1439-2024

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

## Product

Centurion Curette kits labeled as:   a) STERILE BUCK EAR CURETTE "00" (25697), Product Code 66745;   b) STERILE "1" EAR CURETTE (505629), Product Code 67050;   c) STERILE FOX DERMAL CURETTE, 5MM(32923), Product Code 67430;   d) STERILE EXCAVATOR CURETTE (P/S), Product Code I67970;   e) ST BUCK EAR CURETTE BLNT STR SZ 00, Product Code I68040;   f) STERILE BRUNS CURETTE #4 (BC400S), Product Code I68340;   g) 6MM FOX DERMAL CURETTE STERILE, Product Code I68380;   h) STERILE KEVORKIAN CURETTE 4MM (KEC4S), Product Code I68470;   i) ST ENDOCERVICAL BIOPSY CURETTE 2MM, Product Code I68480

## 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-1439-2024
- **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-1439-2024

## Citation

> AI Analytics. FDA recall Z-1439-2024. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1439-2024. Source: US FDA. Licensed CC0.

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