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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