Pulset Arterial Blood Gas — Class II medical device recall Z-0103-2013
Terminated recall by Westmed Inc, reported 2012-10-31, distributed nationwide. Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalli
| Recall number | Z-0103-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Westmed Inc, Tucson, AZ, United States |
| Recall initiated | 2011-01-18 |
| Classified | 2012-10-20 |
| Reported by FDA | 2012-10-31 |
| Terminated | 2012-10-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA, CR, LB, NL, SV |
| Quantity | 1,259,200 units |
| Lot numbers | 43406, 43607, 44030, 44062, 44264, 44327, 44422, 44863, 44981, 45262, 46124, 46585, 46886, 47077, 47312, 48831 |
| Model numbers | 3363-95S |
Product
Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit, Pulset, 3 cc, w/Crickett 23g x 1" A Needle, Luer Slip Barrel, 25U Balanced Heparin, No B Needle or Q-Cork, part number: 3363-95S. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinations.
Reason for recall
Westmed is recalling Westmed ABG convenience kits containing TRIAD brand alcohol pads because TRIAD is recalling TRIAD brand alcohol pads due to potential contaminants.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0103-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.