# FDA recall Z-3006-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-04-08.

## Product

Medline Convenience kits labeled as:   1) COMPREHENSIVE PROCEDURE PACK, Pack Number 7791 ;  2) LAVH CDS, Pack Number CDS760049AC;  3) LAPAROSCOPY CDS , Pack Number CDS760051AB;  4) LAPAROSCOPY CDS , Pack Number CDS760051AC;  5) LAPAROSCOPY CDS , Pack Number CDS760051AD;  6) ABDOMINAL LAPAROSCOPY , Pack Number CDS760057G ;  7) ABDOMINAL LAPAROSCOPY , Pack Number CDS760057I ;  8) ABDOMINAL LAPAROSCOPY , Pack Number CDS760057J ;  9) ABDOMINAL LAPAROSCOPY , Pack Number CDS760057K ;  10) CYSTO PROCEDURE , Pack Number CDS760062P ;  11) CYSTO PROCEDURE , Pack Number CDS760062Q ;  12) LAPAROSCOPY CDS , Pack Number CDS830216F ;  13) FETAL SURGERY CDS-LF, Pack Number CDS840214Q ;  14) MINOR LAPAROTOMY CDS, Pack Number CDS860016P ;  15) MINOR LAPAROTOMY CDS, Pack Number CDS860016Q ;  16) MINOR LAPAROTOMY CDS, Pack Number CDS860016R ;  17) MINOR LAPAROTOMY CDS, Pack Number CDS860016S ;  18) THOROCOTOMY , Pack Number CDS860040I ;  19) LAPAROTOMY CDS #31-RF , Pack Number CDS860062Q ;  20) LAPAROTOMY

## Reason for recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-3006-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **Report date:** 2024-09-18

- **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-3006-2024

## Citation

> AI Analytics. FDA recall Z-3006-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-3006-2024. Source: US FDA. Licensed CC0.

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