Immulite 2500 insulin Kit
FDA device recall Z-0324-05 · posted 2004-12-17 · Terminated
Recall details
- Recalling firm
- Diagnostic Products Corp
- Reason for recall
- Low bias of 10 to 40% at different levels of insulin in samples.
- Action taken
- Customers were notified by telephone on 11/19/2004. They were instructed to discard remaining kits.
- Root cause
- Other
- Status
- Terminated
- Product code
- CFP
- Quantity affected
- 10 kits
- Distribution
- Medical facilities in AK, NY, WI.
- Date initiated
- 2004-11-19
- Date posted
- 2004-12-17
- Date terminated
- 2005-03-24
- Location
- Los Angeles, CA
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