Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit, Pulset, 3 cc, w/Crickett 23g x 1" A Needle, 25U Balanced Heparin, No B Needle or Q-Cork, part number: 3363-95. 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: Lot Numbers: 38637, 38915, 39143, 39147, 39146, 39392, 39745, 39746, 39747, 39748, 40014, 40226, 40225, 40224, 40223, 40565, 40910, 40567, 40955, 41086, 41087, 41317, 41413, 41412, 41414, 41592, 41973, 42071, 42171, 42321, 42595, 42319, 43180, 43130, 43405,43618, 43751, 44064, 44104, 44145, 44384, 44566, 44835, 45057, 45058, 45257, 45255, 45256, 45366, 45669, 45766, 45882, 46108, 46108, 46122, 46339, 46469, 46777, 46655, 46974, 47080, 47226, 47314, 47434, 47596, 47651, 47747, 47746, 48157, 48221, 48483, 48579, 48507, 48623, 48622, 48482, 48762, 48810, 48971, 48927, 49096, 49182, 49259, 49301, 49304, 49303, 49305, 49451, 49586, 49786, 49842.
- 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. Modified Kit, Pulset, 3 cc, w/Crickett 23g x 1" A Needle, 25U Balanced Heparin, No B Needle or Q-Cork, part number: 3363-95. 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:
Lot Numbers: 38637, 38915, 39143, 39147, 39146, 39392, 39745, 39746, 39747, 39748, 40014, 40226, 40225, 40224, 40223, 40565, 40910, 40567, 40955, 41086, 41087, 41317, 41413, 41412, 41414, 41592, 41973, 42071, 42171, 42321, 42595, 42319, 43180, 43130, 43405,43618, 43751, 44064, 44104, 44145, 44384, 44566, 44835, 45057, 45058, 45257, 45255, 45256, 45366, 45669, 45766, 45882, 46108, 46108, 46122, 46339, 46469, 46777, 46655, 46974, 47080, 47226, 47314, 47434, 47596, 47651, 47747, 47746, 48157, 48221, 48483, 48579, 48507, 48623, 48622, 48482, 48762, 48810, 48971, 48927, 49096, 49182, 49259, 49301, 49304, 49303, 49305, 49451, 49586, 49786, 49842.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0101-2013
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.