Drug recall
Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent…
FDA recall event 86429 · Class II · Perrigo Company PLC
Key facts
| Event ID | 86429 |
|---|---|
| Recall numbers | D-1594-2020 |
| Recalling firm | Perrigo Company PLC |
| Product type | Drugs |
| Products | Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma Solutions, 160 N Pharma Drive, Morrisville, NC 27560, Distributed by: Perrigo… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Defective Delivery System: Sustained trend of failure to dispense complaints. |
| Initiation date | Sep 16, 2020 |
| Report date | Sep 30, 2020 |
| Termination date | May 22, 2023 |
| City | Allegan |
| State | MI |
| Country | United States |
| FEI number | 1811666 |
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: