Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0099-2013 — Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit, Pulset, 1 cc, with Eclipse, 25 g x 5/8" A Needle, 25U Balanced Heparin, part number: 3173-98. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinations.

U.S. FDA — Device Enforcement · United States · 2011-01-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0099-2013
Date of alert: 2011-01-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Westmed Inc
Product category: device
Product type: Devices

Reported risk: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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