Albuterol Sulfate Inhalation Aerosol — Class II drug recall D-1594-2020
Terminated recall by Perrigo Company PLC, reported 2020-09-30, distributed nationwide. Defective Delivery System: Sustained trend of failure to dispense complaints.
| Recall number | D-1594-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Perrigo Company PLC, Allegan, MI, United States |
| Recall initiated | 2020-09-16 |
| Classified | 2020-09-23 |
| Reported by FDA | 2020-09-30 |
| Terminated | 2023-05-22 |
| Distributed | Nationwide (US) |
| Quantity | 7,775,813 metered |
| NDC | 45802-0088, 45802-0088-01 |
| Expiration dates | 2020-09, 2020-10, 2020-11, 2020-12, 2021-01, 2021-02, 2021-04, 2021-05, 2021-06, 2021-07, 2021-08, 2021-09, 2022-03, 2022-04, 2022-05, 2022-06 |
Product
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, Allegan, MI 49010 NDC 45802-088-01
Reason for recall
Defective Delivery System: Sustained trend of failure to dispense complaints.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1594-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.