# FDA recall Z-3045-2024

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

## Product

Medline Convenience kits labeled as:    1) GROTH PELVISCOPY CDS, Pack Number CDS984187T ;   2) GROTH PELVISCOPY, Pack Number CDS984187U ;   3) DERMATOLOGY KIT, Pack Number DYNDA1567D;   4) ER MINOR SUTURE SET, Pack Number DYNDA1977A;   5) HSG TRAY, Pack Number DYNDH1453;   6) TRAY, ER LACERATION, Pack Number DYNDL1569A;   7) LAP/PELVISCOPY CSTM PK-LF , Pack Number DYNJ0157511K ;   8) SMSC-PELVISCOPY PACK-LF , Pack Number DYNJ0161619I ;   9) LAPAROSCOPY/PELVISCOPY PACK-LF, Pack Number DYNJ0477038K ;   10) LITHOTOMY/PELVISCOPY PACK , Pack Number DYNJ0531985R ;   11) GYN PELVISCOPY PACK-LF, Pack Number DYNJ0537705L ;   12) SM-PELVISCOPY PACK-LF , Pack Number DYNJ0780009W ;   13) SM-PELVISCOPY PACK-LF , Pack Number DYNJ0780009Y ;   14) PELVISCOPY PACK-LF, Pack Number DYNJ0843760I ;   15) PELVISCOPY PACK-LF, Pack Number DYNJ0843760J ;   16) PELVISCOPY LAP-LF , Pack Number DYNJ40099B ;   17) PELVISCOPY LAP-LF , Pack Number DYNJ40099C ;   18) PELVISCOPY GYN LAP PACK , Pack Number DYNJ40608D ;

## 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-3045-2024
- **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-3045-2024

## Citation

> AI Analytics. FDA recall Z-3045-2024. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-3045-2024. Source: US FDA. Licensed CC0.

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