Recall Z-0632-2013
Horiba Instruments, Inc dba Horiba Medical · initiated October 10, 2012
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
ABX PENTRA AST CP, Part Number: A11A01629. The ABX Pentra AST CP reagent is a diagnostic reagent for quantitative in vitro determination of Aspartate Amino Transferase (AST) in serum or plasma by colorimetry.
Codes / lots: Lot number: 00456-4108
Reason for recall
Horiba Medical is recalling the ABX PENTRA AST CP because during the AST application validation on the Pentra C200 using an Audit Systems linearity kit, it was determined that two higher values for AST (expected at 800 U/L and 1000 U/L) were recorded at 280 and 199 U/L without alarm.
FDA-determined cause: Software design
Action taken
Horiba Medical sent a Field Safety Notification and Acknowledgement Letter dated November 20, 2012, to all affected customers. The letter notified the customers of the problems identified and the actions to be taken. Customers were instructed to complete and return the enclosed response form within 10 calendar days via mail, email or fax. Customers with questions were instructed to contact their local representative. For questions regarding this recall call 714-273-9254.
Details
- Recall number
- Z-0632-2013
- Initiated
- October 10, 2012
- Posted by FDA
- January 3, 2013
- Terminated
- September 12, 2013
- Product code
- CIT – Nadh Oxidation/Nad Reduction, Ast/Sgot
- Quantity
- 66886 units
- Distribution
- Nationwide Distribution including CA, OK, NY, FL, AZ, NY, VA, and TX.
- Recalling firm
- Horiba Instruments, Inc dba Horiba Medical, Irvine, CA
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-0633-2013 Class II | PENTRA C200, Part Number: A11A01629. The Pentra C200 system is a fully automated…Horiba Medical is recalling the ABX PENTRA AST CP because during the AST application validation on the… | 10/10/2012Terminated |