VeriCal Calibrator Set
FDA device recall Z-0032-06 · posted 2005-10-22 · Terminated
Recall details
- Recalling firm
- BIOMERIEUX, INC.
- Reason for recall
- The product is being recalled due to mis-assignment of ISI values associated with VeriCal use.
- Action taken
- Consignees were notified on/about 08/31/2005.
- Root cause
- Other
- Status
- Terminated
- Product code
- JPA
- Quantity affected
- 2334 kits
- Distribution
- Nationwide
- Date initiated
- 2005-08-19
- Date posted
- 2005-10-22
- Date terminated
- 2006-10-16
- Location
- Durham, NC
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