# FDA recall Z-1616-2025

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

## Product

Medline Convenience kits used for various procedures:  1) UTHET TYLER OB PACK, Model Number: DYNJ68673;   2) D AND C PACK, Model Number: DYNJ66290A;   3) D & C PACK-LF, Model Number: DYNJ24159C;   4) OB PACK, Model Number: DYNJ54484A;   5) PERI GYN-LF, Model Number: DYNJS3040;   6) D&C, Model Number: DYNJ900422F;   7) D&C HYSTEROSCOPY CDS, Model Number: CDS985201A;   8) D AND C PACK, Model Number: DYNJ66290A;   9) D&C PACK, Model Number: DYNJ47616B;   10) WMC D & C PACK-LF, Model Number: DYNJ50656B;   11) TRANSVAGINAL PACK, Model Number: DYNJ36599;   12) OB PACK, Model Number: DYNJ25915G;   13) PERI GYN-LF, Model Number: DYNJS3040;   14) MEMORIAL D AND C PACK, Model Number: DYNJ0989660A;   15) HYSTEROSCOPY PACK, Model Number: DYNJ64226A;   16) OB PACK, Model Number: DYNJ64571;   17) WMC D & C PACK-LF, Model Number: DYNJ50656B;   18) D & C PACK-LF, Model Number: DYNJT2535G;   19) OB PACK, Model Number: DYNJ44522B;   20) OB PACK-LF, Model Number: DYNJ26121G;   21) NYGH-HYSTEROSCOPY-LF, M

## 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-1616-2025
- **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-1616-2025

## Citation

> AI Analytics. FDA recall Z-1616-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1616-2025. Source: US FDA. Licensed CC0.

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