# FDA recall Z-1600-2025

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

## Product

Medline Convenience kits used for various procedures:  1) OCULOPLASTIC PICK PACK, Model Number: DYNJ43914B;   2) PLASTIC PACK, Model Number: DYNJ65109;   3) PLASTIC PROCEDURE PACK, Model Number: DYNJ34160D;   4) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   5) PLASTIC PACK, Model Number: DYNJ66056;   6) MUSCLE PLASTIC PACK, Model Number: DYNJ66212A;   7) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   8) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   9) GENERAL BREAST GRH-LF, Model Number: DYNJ52658D;   10) FACE PACK, Model Number: DYNJ37316D;   11) PLASTIC PACK-LF, Model Number: DYNJ57440D;   12) MINOR BREAST SJHC-LF, Model Number: DYNJ84991;   13) MINOR PLASTIC PACK, Model Number: DYNJ37231B;   14) SATELLITE MINOR PLASTIC PACK, Model Number: DYNJ63696;   15) FACIAL/EYE PACK, Model Number: DYNJ68328;   16) BREAST PACK, Model Number: DYNJ63753;   17) BREAST PACK, Model Number: DYNJ63753;   18) TUMMY PACK, Model Number: DYNJ64886A;   19) PLASTIC TORSO PK TEGH-LF, Model Number: DY

## 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-1600-2025
- **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-1600-2025

## Citation

> AI Analytics. FDA recall Z-1600-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1600-2025. Source: US FDA. Licensed CC0.

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