# FDA recall Z-1122-2019

> **Becton Dickinson & Company** · Class II · device recall initiated 2019-03-07.

## Product

BD Blood Collection Assembly with Male Luer Lock, Catalog Number MBC6010

## Reason for recall

The luer could break and cause the device to leak or break off and get stuck in the fistula needle port rendering the port inaccessible for dialysis.  As a result, the patient would need to be re-cannulated with a new fistula needle to obtain their dialysis treatment.

## Distribution

US distribution to the states of FL and NJ.

## Key facts

- **Recall number:** Z-1122-2019
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-07
- **Report date:** 2019-04-17
- **Termination date:** 2020-05-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Franklin Lakes, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1122-2019

## Citation

> AI Analytics. FDA recall Z-1122-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1122-2019. Source: US FDA. Licensed CC0.

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