Known Identifiers & Locations
FEI Numbers
1924669
Owner Operator Numbers
N/A
Locations Covered
N/A
Registered Establishments (0)
No device registration and listing records found for this entity.
510(k) Premarket Notifications (0)
No 510(k) notifications found for this entity.
FDA Recall History (1)
| Recall # |
Product Description |
Initiation Date |
Status |
Action |
| Z-0024-05 |
Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro diagnostic use. The firm name on the label is Remel, Lenexa, KS.
Reason: The product does not perform as intended with some quality control organisms (Haemophilus influenzae)
|
2004-09-27 |
Terminated
|
View Details
|
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