# FDA recall Z-1444-2025

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

## Product

Medline procedure kits labeled as:   1) A & A KNEE PACK-LF, Pack Number DYNJHS0136D;  2) ABD CLOSURE PACK, Pack Number DYNJ56987B;  3) ADULT PERC PACK-LF, Pack Number PHS170994005A;  4) BASIC PACK, Pack Number DYNJ54836B;  5) BASIC PACK, Pack Number DYNJ58678A;  6) BASIC PACK, Pack Number DYNJ63532;  7) BASIC PACK, Pack Number DYNJ81702;  8) BASIC PACK, Pack Number DYNJ36595D;  9) BASIC PACK, Pack Number DYNJ69250A;  10) BEACH CHAIR SHOULDER PACK, Pack Number DYNJ50470C;  11) BGMC ADULT HERNIA PACK-LF, Pack Number DYNJ0115839A;  12) BMT EP PROCEDURE PACK-LF, Pack Number PHS396134006A;  13) CABG PACK, Pack Number DYNJ20114Q;  14) CABG UNIVERSITY HOSP PACK-LF, Pack Number DYNJ0375705L;  15) CHEST PACK SC-LF, Pack Number DYNJ38051F;  16) CHOM START UP PACK-LF, Pack Number DYNJ0161358B;  17) CHS RFT TOTAL KNEE PACK, Pack Number DYNJ50844B;  18) COMPOSITE NECK DISSEC SHSC-LF, Pack Number DYNJ46776C;  19) COMPOSITE RESECTION PACK, Pack Number DYNJ40640B;  20) CSTM PK DRP SURG MIN PK LGRAY, P

## 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-1444-2025
- **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-1444-2025

## Citation

> AI Analytics. FDA recall Z-1444-2025. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/Z-1444-2025. Source: US FDA. Licensed CC0.

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