# FDA recall Z-1617-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-03-03.

## Product

Medline Convenience kits used for various procedures:  1) BASIC CATARACT, Model Number: DYNJ41097A;   2) PK EYE, Model Number: DYNJ60631B;   3) CATARACT PACK, Model Number: DYNJ80316A;   4) BASIC EYE PACK, Model Number: DYNJ63707C;   5) EYE PACK WITH ACCESSORY PACK, Model Number: DYNJ85284;   6) PHACO PACK, Model Number: DYNJ44748I;   7) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   8) CHOG MINOR OPHTHALMIC PACK, Model Number: SYNJ10271B;   9) LIFESPAN VITRECTOMY PACK, Model Number: DYNJ80082;   10) DR KEYS EYE PACK 2, Model Number: DYNJ48256M;   11) VITRECTOMY PACK, Model Number: DYNJ55508B;   12) EYE PACK, Model Number: DYNJ63952A;   13) VITRECTOMY, Model Number: DYNJ67309C;   14) CATARACT PACK-MARY IMMACUL-LF, Model Number: DYNJ24516F;   15) DR FLOOD EYE PACK, Model Number: DYNJ57258G;   16) BLEPH PACK, Model Number: DYNJ67875;   17) CAROMONT EYE TRAY-LF, Model Number: DYNJ17004L;   18) EYE PLASTIC PACK, Model Number: DYNJ47859C;   19) OPHTHALMOLOGY PACK, Model Number: SYNJ10259

## Reason for recall

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

## Key facts

- **Recall number:** Z-1617-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-03
- **Report date:** 2025-04-23

- **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-1617-2025

## Citation

> AI Analytics. FDA recall Z-1617-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1617-2025. Source: US FDA. Licensed CC0.

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