# FDA recall Z-2067-2019

> **Medline Industries Inc** · Class I · device recall initiated 2019-05-10.

## Product

Centurion Convenience Kits, containing BD Alaris Pump Infusion Sets. BD code 11522558 (Centurion code 110931) contained inside kits DYNJ52509A and DYNJ52510A.    Product Usage:  The Centurion Primary Set Pack and Primary Warmer Pack Convenience Kit helps continuously or intermittently deliver fluids, medications, blood and blood products to adult, pediatric or neonatal patients.

## Reason for recall

This recall is a sub recall to BD s recent Class I recall for the Alaris Pump Infusion Set due to an issue with the consistency of the inner lumen thickness of the silicone tubing segment which directly impacts amount of occlusion force necessary to fully seal the tube. This defect prevents the pump from complete occlusion and results in the potential for over-infusion of drug product into the patient.

## Distribution

One distributor located in Illinois.

## Key facts

- **Recall number:** Z-2067-2019
- **Recalling firm:** Medline Industries Inc
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-10
- **Report date:** 2019-08-21
- **Termination date:** 2021-08-18

- **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-2067-2019

## Citation

> AI Analytics. FDA recall Z-2067-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2067-2019. Source: US FDA. Licensed CC0.

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