# FDA recall Z-2663-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2020-06-19.

## Product

PowerLoc MAX Power Injectable Infusion Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit; Catalog Numbers 2132010G (UDI 00801741095504), 2132015G (UDI 00801741095511), 2141910G (UDI 00801741095542), 2142010G (UDI 00801741085680), 2142015G (UDI 00801741085680), 2142210G (UDI 00801741085680)

## Reason for recall

Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.

## Distribution

Worldwide Distribution

## Key facts

- **Recall number:** Z-2663-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-19
- **Report date:** 2020-07-29
- **Termination date:** 2022-07-29

- **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-2663-2020

## Citation

> AI Analytics. FDA recall Z-2663-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2663-2020. Source: US FDA. Licensed CC0.

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