# FDA recall Z-0141-2024

> **Smiths Medical ASD Inc.** · Class II · device recall initiated 2023-09-06.

## Product

Portex Pro-Vent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF 4599P-1

## Reason for recall

The complaint involved the absence of a component called "ASM Filter-Pro ABG SYR CAP" from the packaging of Pro-Vent Arterial Blood Sampling (ABG) Kits. Specifically, this issue affected a total of 31,900 kits under the FGSKU# 4599P-1 and Lot# 4331283. Tubes without caps have the potential to generate delayed or erroneous test results and/or exposure to infectious blood.

## Distribution

US

## Key facts

- **Recall number:** Z-0141-2024
- **Recalling firm:** Smiths Medical ASD Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-06
- **Report date:** 2023-11-01

- **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-0141-2024

## Citation

> AI Analytics. FDA recall Z-0141-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0141-2024. Source: US FDA. Licensed CC0.

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