# FDA recall Z-2701-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-03-22.

## Product

Medline medical procedure kits labeled as follows:    a) HEART ANESTHESIA SET UP, REF DYNJ902752C,   b) KIT ENDO, REF DYKE1872A,   c) LOWER ENDO KIT, REF DYKE1921A,   d) PACEMAKER, REF DYNJ901681D,   e) UPPER ENDO KIT, REF DYKE1922A,   f) VASCULAR, REF DYNJ905515D,   g) VASCUALR, REF DYNJ902387K,   h) VASCULAR III, REF DYNJS2035C

## Reason for recall

A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

## Distribution

Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.

## Key facts

- **Recall number:** Z-2701-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-22
- **Report date:** 2024-08-28

- **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-2701-2024

## Citation

> AI Analytics. FDA recall Z-2701-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2701-2024. Source: US FDA. Licensed CC0.

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