# FDA recall Z-0177-2025

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

## Product

Medline brand medical procedure convenience kits, labeled as:    a) OB PACK-LF, REF DYNJ0912449M;   b) OB PACK, REF DYNJ17309G;   c) OB PK, REF DYNJ34268D;   d) OB DELIVERY PACK, REF DYNJ34274B;   e) OB DELIVERY PACK, REF DYNJ34274B;   f) D AND C PACK, REF DYNJ39668I;   g) OB PACK, REF DYNJ42884;   h) RFT D & C PACK, REF DYNJ50851;   i) KIT OB, REF DYNJ906623;   j) D AND C, REF DYNJ907957A;   k) CHS OB PACK III, REF DYNJCH907

## 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-0177-2025
- **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-0177-2025

## Citation

> AI Analytics. FDA recall Z-0177-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0177-2025. Source: US FDA. Licensed CC0.

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