# FDA recall Z-1465-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2025-02-11.

## Product

Medline procedure kits labeled as:   1) ACL ARTHROSCOPY PACK, Pack Number DYNJ55316G;  2) ARTERIOGRAM PACK, Pack Number DYNJ64332;  3) ARTHRO PACK-LF, Pack Number DYNJ38748F;  4) ARTHRO PACK-LF, Pack Number DYNJ38748F;  5) ARTHROGRAM PACK, Pack Number DYNJ65817;  6) ARTHROGRAM TRAY, Pack Number DYNDH1937;  7) ARTHROSCOPY KNEE PACK-LF, Pack Number DYNJ0809731F;  8) ARTHROSCOPY PACK, Pack Number DYNJ66665;  9) ARTHROSCOPY PACK, Pack Number DYNJ38716C;  10) ARTHROSCOPY PACK, Pack Number DYNJ33639J;  11) ARTHROSCOPY PACK, Pack Number DYNJ37707D;  12) ARTHROSCOPY PACK, Pack Number DYNJ38914A;  13) ARTHROSCOPY PACK, Pack Number DYNJ64526A;  14) ARTHROSCOPY PACK, Pack Number DYNJ62755B;  15) ARTHROSCOPY PACK, Pack Number DYNJ61634B;  16) ARTHROSCOPY PACK, Pack Number DYNJ83129;  17) ARTHROSCOPY PACK, Pack Number DYNJ35906F;  18) ARTHROSCOPY PACK, Pack Number DYNJ35906F;  19) ARTHROSCOPY PACK, Pack Number DYNJ37946C;  20) ARTHROSCOPY PACK, Pack Number DYNJ68133A;  21) ARTHROSCOPY PACK BCS, Pac

## Reason for recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.

## Distribution

Worldwide distribution - US Nationwide and the country of Canada.

## Key facts

- **Recall number:** Z-1465-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-11
- **Report date:** 2025-04-02

- **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-1465-2025

## Citation

> AI Analytics. FDA recall Z-1465-2025. Retrieved 2026-08-01 from https://api.ai-analytics.org/recall/Z-1465-2025. Source: US FDA. Licensed CC0.

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