Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit, Pulset, 3 cc, 23g x 1" A/B Needle, 25U Balanced Heparin, part numbers: 3373, 3393. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinations.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Part Number 3373, Lot Numbers: 38813, 38634, 39148, 39946, 40951, 40952, 41593, 41740, 42914, 43291, 43999, 45252, 46341, 46653, 47175, 47371, 48029, 48266, 48351, 48495, 48661, 48897, 49145, 49236, 49325, 49408, 49522, 49718, 49966. Part Number: 3393, Lot numbers: 38995, 33994, 39788, 40082, 40568, 40569, 40674, 40994, 41325, 41326, 41749, 41931, 44536, 44534, 44535, 44533.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Westmed Inc
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit, Pulset, 3 cc, 23g x 1" A/B Needle, 25U Balanced Heparin, part numbers: 3373, 3393. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient for blood gas determinations.
Product Codes/Lot Numbers:
Part Number 3373, Lot Numbers: 38813, 38634, 39148, 39946, 40951, 40952, 41593, 41740, 42914, 43291, 43999, 45252, 46341, 46653, 47175, 47371, 48029, 48266, 48351, 48495, 48661, 48897, 49145, 49236, 49325, 49408, 49522, 49718, 49966. Part Number: 3393, Lot numbers: 38995, 33994, 39788, 40082, 40568, 40569, 40674, 40994, 41325, 41326, 41749, 41931, 44536, 44534, 44535, 44533.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0106-2013
Related Recalls
Due to connector within the circuit flex extender not meeting specifications resulting in a low connection force and as a result, the connector may leak or disconnect and may cause life threating conditions or death.
There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.