🔍 RecallPedia

Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit, Pulset, 3 cc, w/Crickett 22g x 1", 25U Balanced Heparin, part number: 3362-95. 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 - Dangerous
🏥 Medical Devices Recalled: January 18, 2011 Westmed Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Numbers: 39560, 39833, 40185, 40201, 40332, 40983, 41027, 41253, 41693, 41884, 42224, 42592, 42977, 43290, 43373, 43564, 43670, 43752, 44143, 44333, 44677, 44752, 45212, 45559, 45560, 45699, 46107, 46356, 46271, 46654, 46923, 47078, 47218, 47774, 48288, 48143.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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, w/Crickett 22g x 1", 25U Balanced Heparin, part number: 3362-95. 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: 39560, 39833, 40185, 40201, 40332, 40983, 41027, 41253, 41693, 41884, 42224, 42592, 42977, 43290, 43373, 43564, 43670, 43752, 44143, 44333, 44677, 44752, 45212, 45559, 45560, 45699, 46107, 46356, 46271, 46654, 46923, 47078, 47218, 47774, 48288, 48143.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0102-2013

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