# FDA recall Z-3046-2024

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

## Product

Medline Convenience kits labeled as:   1) LAVH CDS, Pack Number CDS760049AB;  2) TUBAL LIGATION CDS, Pack Number CDS760053D ;  3) TUBAL LIGATION CDS, Pack Number CDS760053G ;  4) TUBAL LIGATION CDS, Pack Number CDS760053I ;  5) TUBAL LIGATION CDS, Pack Number CDS760053J ;  6) GYN LAPAROSCOPY-LF, Pack Number CDS760059F ;  7) GYN LAPAROSCOPY-LF, Pack Number CDS760059G ;  8) GYN LAPAROSCOPY-LF, Pack Number CDS760059I ;  9) GYN LAPAROSCOPY-LF, Pack Number CDS760059J ;  10) LIVER TRANSPLANT #57 CDS-2, Pack Number CDS860063R ;  11) GYN LAP , Pack Number CDS860087L ;  12) GYN LAPAROSCOPY CDS , Pack Number CDS860119Q ;  13) GYN LAPAROSCOPY CDS , Pack Number CDS860119R ;  14) GYN LAPAROSCOPY CDS , Pack Number CDS860119S ;  15) GYN LAPAROSCOPY CDS , Pack Number CDS860119U ;  16) GYN LAPAROSCOPY-LF, Pack Number CDS920074X ;  17) GYN LAPAROSCOPY CDS #34-RF, Pack Number CDS920099Q ;  18) GYN LAPAROSCOPY CDS #34-RF, Pack Number CDS920099R ;  19) GYN LAPAROSCOPY CDS #34-RF, Pack Number CDS920099S ;  

## 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-3046-2024
- **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-3046-2024

## Citation

> AI Analytics. FDA recall Z-3046-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-3046-2024. Source: US FDA. Licensed CC0.

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