# FDA recall Z-2764-2024

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

## Product

Medline procedural kits labeled as:   1) ALL DOC EYE PACK, Pack Number DYNJ51654A ;  2) ASC CATARACT PACK , Pack Number DYNJ0855117O ;  3) BAI , Pack Number DYNJ53847D ;  4) BASIC EYE PACK, Pack Number DYNJ83699A ;  5) BASIC EYE PACK, Pack Number DYNJ81805;  6) BASIC EYE PACK, Pack Number DYNJ83699A ;  7) BYERS CATARACT, Pack Number DYNJ67344;  8) BYERS CATARACT, Pack Number DYNJ67344H ;  9) CATARACT, Pack Number DYNJ44544B ;  10) CATARACT, Pack Number DYNJ54713C ;  11) CATARACT CDS , Pack Number CDS983804F ;  12) CATARACT CDS, Pack Number CDS983804F ;  13) CATARACT DR MALONE PACK , Pack Number DYNJ51590A ;  14) CATARACT DR MULROONEY PACK, Pack Number DYNJ51595A ;  15) CATARACT DR STEVENS PACK, Pack Number DYNJ51593C ;  16) CATARACT L J, Pack Number DYNJ40056A ;  17) CATARACT PACK, Pack Number CMPJ03235C ;  18) CATARACT PACK, Pack Number DYNJ80316A ;  19) CATARACT PACK, Pack Number VAL011CTASF;  20) CATARACT PACK , Pack Number CMPJ03235C ;  21) CATARACT PACK , Pack Number DYNJ31020K ; 

## 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

## Key facts

- **Recall number:** Z-2764-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-08
- **Report date:** 2024-09-04

- **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-2764-2024

## Citation

> AI Analytics. FDA recall Z-2764-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2764-2024. Source: US FDA. Licensed CC0.

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