# FDA recall Z-1451-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-02-11.

## Product

Medline procedure kits labeled as:    1) AOP/BASIC EYE PACK-LF, Pack Number DYNJ0589795V;   2) CATARACT CM-LF, Pack Number DYNJ39921B;   3) CATARACT EYE, Pack Number DYNJ45662C;   4) CATARACT PACK, Pack Number DYNJ56056B;   5) CATARACT PACK, Pack Number DYNJ56553B;   6) CATARACT PACK, Pack Number DYNJ0417156G;   7) CATARACT PACK, Pack Number DYNJ60411A;   8) CATARACT PACK, Pack Number DYNJ52649F;   9) CATARACT PACK - 30843, Pack Number DYNJVB1076B;   10) CATARACT PACK-LF, Pack Number DYNJ0317858M;   11) CATARACT-LF, Pack Number DYNJ40081F;   12) ENT PACK, Pack Number DYNJ38916B;   13) EYE CATARACT PK, Pack Number DYNJ46557K;   14) EYE CATARACT PK, Pack Number DYNJ46557L;   15) EYE PACK, Pack Number DYNJ48800C;   16) EYE PACK, Pack Number DYNJ38494G;   17) EYE PACK, Pack Number DYNJ21134A;   18) EYE PACK 1, Pack Number DYNJHTEY01;   19) EYE PACK II-LF, Pack Number DYNJ50237A;   20) EYE PBM-LF, Pack Number DYNJ0190619G;   21) MZ GENERAL EYE PACK, Pack Number DYNJ66623A;   22) OCULAR PLAS

## 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 - US Nationwide and the country of Canada.

## Key facts

- **Recall number:** Z-1451-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-11
- **Report date:** 2025-04-02

- **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-1451-2025

## Citation

> AI Analytics. FDA recall Z-1451-2025. Retrieved 2026-09-08 from https://api.ai-analytics.org/recall/Z-1451-2025. Source: US FDA. Licensed CC0.

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