Drug recall
HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile…
FDA recall event 82718 · Class II · Advanced Pharma Inc.
Key facts
| Event ID | 82718 |
|---|---|
| Recall numbers | D-1251-2019 |
| Recalling firm | Advanced Pharma Inc. |
| Product type | Drugs |
| Products | HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877)… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Sub-potency |
| Initiation date | Apr 26, 2019 |
| Report date | May 8, 2019 |
| Termination date | Oct 30, 2019 |
| City | Houston |
| State | TX |
| Country | United States |
| FEI number | 3005247494 |
At a glance
- 1–9 Products in this recall
- 1–9 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: