# FDA recall Z-2613-2026

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

## Product

Medline Convenience kits containing recalled Swan-Ganz Catheters    CABG A CDS	  	CDS982269K  	CDS982269L  	CDS982269M  	CDS982269N  	  CARDIAC MAJOR	  	DYNJ901328D  	DYNJ901328F  	  HEART A	  	DYNJ903465F  	DYNJ903465G  	  HEART TRAY-VASCULAR	  	DYNJ907857  	DYNJ907857A  	DYNJ907857B  	  KIT UNIVERSITY CABG PK	  	DYNJ905857A  	  OPEN HEART	  	CDS981161AA  	CDS981161AB  	DYNJ905437A  	DYNJ909090  	DYNJ909090C  	DYNJ9855016R  	DYNJ9855016S  	  OPEN HEART ACCESSORY CDS	  	CDS984289J  	  OPEN HEART ANESTHESIA PACK	  	CDS983849D  	CDS983849F  	CDS983849G  	  OPEN HEART B CDS	  	DYNJ900377P  	  OPEN HEART BASIC B	  	DYNJ904311C  	  OPEN HEART CDS	  	CDS983513F  	  OPEN HEART CDS QVH	  	CDS982523K  	CDS982523L  	CDS982523N  	  OPEN HEART LINE SET UP	  	DYNJ908179  	DYNJ908179A  	  OPEN HEART SUPPLEMENT	  	DYNJ909116  	DYNJ909116A  	DYNJ909116C  	DYNJ909116D  	  SILVER CROSS OPEN HEART	  	DYNJ906102J  	DYNJ906102K  	DYNJ906102L  	  	  SM OPEN HEART PACK A&B	  	DYNJ904749G  	DYNJ904749J  	  VPH OPEN HEART	  	DYNJ902664J  	DYNJ902664K  	DYNJ902664L

## 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-2613-2026
- **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-2613-2026

## Citation

> MORVS. FDA recall Z-2613-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-2613-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*