NEONATAL TOTAL GALACTOSE KIT Product Numbers: 3029-0010, 3029-001B. This kit is intended for the quantitative determination of total galactose (galactose and galactose-1-phosphate) concentrations in blood specimens dried on filter paper as an aid in screening newborns for galactosemia.

Class I - Dangerous

🏥 Medical Devices Recalled: November 26, 2012 Perkinelmer Infusion Pumps Nationwide

What Should You Do?

Check if you have this product:
Lot Numbers: 618201, 619200, 618263
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:: Perkinelmer
Reason for Recall:: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: terminated

Product Information

Full Description:

NEONATAL TOTAL GALACTOSE KIT Product Numbers: 3029-0010, 3029-001B. This kit is intended for the quantitative determination of total galactose (galactose and galactose-1-phosphate) concentrations in blood specimens dried on filter paper as an aid in screening newborns for galactosemia.

Product Codes/Lot Numbers:

Lot Numbers: 618201, 619200, 618263

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0688-2013

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