# FDA recall Z-2612-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-05-28.

## Product

Medline Convenience kits containing recalled Swan-Ganz Catheters    RIGHT HEART CATH PACK CTX	  	DYNJ68530A

## Reason for recall

Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.

## Distribution

US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.

## Key facts

- **Recall number:** Z-2612-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-28
- **Report date:** 2026-07-08

- **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-2612-2026

## Citation

> MORVS. FDA recall Z-2612-2026. Retrieved 2026-10-17 from https://api.morvs.ai/recall/Z-2612-2026. Source: US FDA. Licensed CC0.

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