# FDA recall Z-3051-2024

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

## Product

Medline Convenience kits labeled as:   1) ADULT DRAWER 5, Pack Number ACC010647A ;  2) TUBAL LIGATION CDS, Pack Number CDS760053K ;  3) CATARACT CDS, Pack Number CDS810010J ;  4) CATARACT CDS, Pack Number CDS810010K ;  5) RETINA-LF, Pack Number CDS810023G;  6) RETINA-LF, Pack Number CDS810023I;  7) RETINA-LF, Pack Number CDS810023J;  8) RETINA-LF, Pack Number CDS810023K;  9) EYE CDS , Pack Number CDS810032L ;  10) EYE CDS , Pack Number CDS810032M ;  11) EYE CDS , Pack Number CDS810032N ;  12) EYE CDS , Pack Number CDS810032O ;  13) GENERAL EYE , Pack Number CDS981693I ;  14) GENERAL EYE , Pack Number CDS981693J ;  15) EYE CDS II, Pack Number CDS981738A ;  16) MUSCLE/EYE CDS, Pack Number CDS982059F ;  17) MUSCLE/EYE CDS, Pack Number CDS982059G ;  18) MUSCLE/EYE CDS, Pack Number CDS982059I ;  19) CATARACT CDS-4, Pack Number CDS983001F ;  20) VITRECTOMY CDS-4, Pack Number CDS983005F ;  21) PTERYGIUM CDS , Pack Number CDS983261D ;  22) PTERYGIUM CDS , Pack Number CDS983261F ;  23) PTERYGIU

## 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-3051-2024
- **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-3051-2024

## Citation

> AI Analytics. FDA recall Z-3051-2024. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-3051-2024. Source: US FDA. Licensed CC0.

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