Drug recall
Phenylbutazone 20% Injection 200 mg/ ml - 100 ml glass vials packed in cartons of 12 (ANADA 200-371)…
FDA recall event 73769 · Class III · Sparhawk Laboratories Inc
Key facts
| Event ID | 73769 |
|---|---|
| Recall numbers | V-0015-2017 |
| Recalling firm | Sparhawk Laboratories Inc |
| Product type | Veterinary |
| Products | Phenylbutazone 20% Injection 200 mg/ ml - 100 ml glass vials packed in cartons of 12 (ANADA 200-371) manufactured by Sparhawk Laboratories, Inc. Lenexa, KS 66215. Distributed under the following… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The product pH was found to be out of specification at the 6-month stability time point. |
| Initiation date | Apr 6, 2016 |
| Report date | Nov 23, 2016 |
| Termination date | Apr 3, 2017 |
| City | Lenexa |
| State | KS |
| Country | United States |
| FEI number | 1910619 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: