Home › ASTORIA-PACIFIC, INC. › SPOTCHECK
SPOTCHECK
ASTORIA-PACIFIC, INC. · Model 80-3500-13K · UDI-DI 00725609000038
JBL
Prescription
1
510(k) clearances
0
Adverse events
2
Recalls
3
Facilities
Description
G6PD 25 Hour Reagent Kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-04-03 | Randox Laboratories Ltd. | The target values and ranges in these lots are incorrect. |
| 2019-04-03 | Randox Laboratories Ltd. | The target values and ranges in these lots are incorrect. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.