# FDA recall Z-2103-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-01-07.

## Product

Medline Convenience Kits:  1) CENTRAL LINE UNIVERSAL INSERTI, Model Number: CVI3780;   2) LVAD DRIVELINE TRAY, Model Number: DM1035;   3) KIT SURG ONC INSERT CENT.VENOU, Model Number: DYKMBNDL43

## Reason for recall

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-2103-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-07
- **Report date:** 2026-05-13

- **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-2103-2026

## Citation

> AI Analytics. FDA recall Z-2103-2026. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-2103-2026. Source: US FDA. Licensed CC0.

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