# FDA recall Z-2499-2020

> **Smiths Medical ASD Inc.** · Class II · device recall initiated 2020-06-11.

## Product

PORT-A-CATH¿ II POWER P.A.C. Low Profile" system.

## Reason for recall

Smiths Medical became aware that one (1) lot of PORT-A-CATH¿ II POWER P.A.C. Low Profile" System (SKU 21-4477-24) was packaged with an 8Fr catheter instead of a 6Fr catheter.

## Distribution

Domestic Distribution: AR, CT, MS,TN,TX

## Key facts

- **Recall number:** Z-2499-2020
- **Recalling firm:** Smiths Medical ASD Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-11
- **Report date:** 2020-07-15
- **Termination date:** 2021-01-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Minneapolis, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2499-2020

## Citation

> AI Analytics. FDA recall Z-2499-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2499-2020. Source: US FDA. Licensed CC0.

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