MagNA Pure LC Instrument; catalog numbers 2236931 and 03670325001.
FDA device recall Z-1371-04 · posted 2004-08-17 · Terminated
Recall details
- Recalling firm
- Roche Diagnostics Corp.
- Reason for recall
- A hardware/software problem will result in low elution volumes and bias sample results for various protocols.
- Action taken
- Consignees were notified via recall letter dated 8/6/04.
- Root cause
- Other
- Status
- Terminated
- Product code
- NPQ
- Quantity affected
- 192
- Distribution
- United States.
- Date initiated
- 2004-08-06
- Date posted
- 2004-08-17
- Date terminated
- 2005-10-05
- Location
- Indianapolis, IN
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