# FDA recall Z-0174-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-09-04.

## Product

Medline brand medical procedure convenience kits, labeled as:  1) L&D/OB PACK-LF, REF DYNJ0213264O;   2) VAG DELIVERY HLTH ALLIA PK-LF, REF DYNJ0375486K;   3) VAG DELIVERY HLTH ALLIA PK-LF, REF DYNJ0375486K;   4) VAGINAL DELIVERY, REF DYNJ04865M;   5) VAGINAL DELIVERY PACK-LF, REF DYNJ0536939R;   6) LABOR & DELIVERY-LF, REF DYNJ07831F;   7) DELIVERY PACK-LF, REF DYNJ09982A;   8) DELIVERY PACK-LF, REF DYNJ09982A;   9) DELIVERY ROOM PACK, REF DYNJ14193C;   10) OB PACK, REF DYNJ17486I;   11) OB PACK, REF DYNJ17486I;   12) DELIVERY PACK, REF DYNJ24339K;   13) DELIVERY PACK, REF DYNJ26935A;   14) DELIVERY PACK, REF DYNJ26935A;   15) OB/DELIVERY ROOM PACK, REF DYNJ27262F;   16) VAGINAL DELIVERY TRAY, REF DYNJ27275;   17) VAGINAL DELIVERY, REF DYNJ28437F;   18) OB PACK, REF DYNJ31817K;   19) OB PACK, REF DYNJ31817K;   20) OB PACK, REF DYNJ36010F;   21) OB PACK, REF DYNJ38804G;   22) VAGINAL PACK, REF DYNJ40037A;   23) VAGINAL DELIVERY, REF DYNJ40170A;   24) VAG RECTAL PACK BWH-LF, REF DYNJ416

## Reason for recall

It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.

## Distribution

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

## Key facts

- **Recall number:** Z-0174-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-09-04
- **Report date:** 2024-10-30

- **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-0174-2025

## Citation

> AI Analytics. FDA recall Z-0174-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0174-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*