# FDA recall Z-0122-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-08-28.

## Product

MEDLINE OPEN HEART, REF DYNJ904261B

## Reason for recall

Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0122-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-28
- **Report date:** 2024-10-23

- **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-0122-2025

## Citation

> AI Analytics. FDA recall Z-0122-2025. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0122-2025. Source: US FDA. Licensed CC0.

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