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Histochemical PAS (Periodic Acid Schiff) Reaction Set. in vitro diagnostic. Product size configuration: Set of 4 bottles

FDA device recall Z-0305-2007 · posted 2006-12-27 · Terminated

Recall details

Recalling firm
EMD Chemicals Inc
Reason for recall
Due to loose caps, the SO2 levels dropped significantly from release levels causing the product not to perform properly.
Action taken
On July 27, 2006 EMD contacted its direct account customers via letter. The firm requested discontinue use of the product and contact EMD for return.
Root cause
Other
Status
Terminated
Product code
KKS
Quantity affected
74 kits
Distribution
Nationwide.
Date initiated
2006-07-25
Date posted
2006-12-27
Date terminated
2008-10-06
Location
Gibbstown, NJ

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