# FDA recall Z-1550-2021

> **Bard Peripheral Vascular Inc** · Class II · device recall initiated 2021-03-25.

## Product

PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF 1829500, UDI: (01) 00801741027185 - Product Usage: The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples.

## Reason for recall

Catheters may experience difficulty in flushing, infusion, and/or aspiration, and septum dislodgements.

## Distribution

US Nationwide distribution in the states of AL, AR, AZ, CA, CO,   CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN  MO, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV.

## Key facts

- **Recall number:** Z-1550-2021
- **Recalling firm:** Bard Peripheral Vascular Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-03-25
- **Report date:** 2021-05-19
- **Termination date:** 2023-04-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tempe, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1550-2021

## Citation

> AI Analytics. FDA recall Z-1550-2021. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-1550-2021. Source: US FDA. Licensed CC0.

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