RecallDepth

Pointe Scientific Liquid Auto HDL Cholesterol Reagent Set, Pointe Scientific, Inc., Canton, MI, Catalog Numbers: 10-H7545-80, 12-H7545-162, 3-H7545-L, 7-H7545-1000, 7-H7545-320, 7-H7545-40, 7-H7545-80, H7545-1000, H7545-320, H7545-40, H7545-80, HH945-240 and HH945-480. The product is used for In vitro diagnostic for the quantitative determination of high-density lipoprotein cholesterol in human serum or plasma.

This recall has been terminated (originally issued April 27, 2009).

Company
Pointe Scientific, Inc.
Recall Initiated
January 29, 2009
Posted
April 27, 2009
Terminated
October 20, 2010
Recall Number
Z-1201-2009
Quantity
717 kits, 164L
Firm Location
Canton, MI
Official Source
View on FDA website ↗

Reason for Recall

The R1 reagent has microbial contamination.

Distribution

Worldwide Distribution -- US, Chile, Dominican Republic, Egypt, Ghana, Greece, India, Israel, Italy, Jamaica-West Indies, Korea, Malaysia, Mexico, Philippines, Poland, Romania, Serbia, Trinidad-West Indies, Turkey and Venezuela.

Lot / Code Info

Lot Number: 818202, exp. 12/09.

Root Cause

Nonconforming Material/Component

Action Taken

Consignees were notified by "Urgent: Medical Device Recall" letter dated January 29, 2009, to conduct the recall to the retail level, to examine inventory and dispose of affected stocks on hand, and to complete the "Recall Return Response Form". Consignees were instructed to return their completed forms via mail, fax (1-734-483-1592) or e-mail to Pointe Scientific, Inc. (PS). Direct questions about the recall to PS Technical Support Department at 1-800-757-5313 or 1-734-487-8300.

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