# FDA recall Z-0533-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-10-15.

## Product

(1) Medline Pacer Implant Pack, REF DYNJ59194A, 4 kits/case, sterile; and  (2) Medline Thoracotomy Morristown, REF DYNJ904220F, 1 kit/case, non-sterile.

## Reason for recall

Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.

## Distribution

US Nationwide distribution in the states of AL, GA, MA, NJ, and PA.

## Key facts

- **Recall number:** Z-0533-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-15
- **Report date:** 2024-12-04

- **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-0533-2025

## Citation

> AI Analytics. FDA recall Z-0533-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0533-2025. Source: US FDA. Licensed CC0.

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