Smiths Medical ASD Inc.: Medical Device Recall in 2023 - (Recall #: Z-0141-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 6, 2023

Date Posted: November 1, 2023

Recall Number: Z-0141-2024

Event ID: 93094

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.

Status: Ongoing

Product Quantity: 31900 devices

Code Information:

UDI/DI 30351688028635, Lot Number 4331283

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated