Drug recall
Albuterol 0.083% Inh Sol. 30 days supply, Rx Only, 39183, NDC 76204-0200-60, 30
FDA recall event 79748 · Class II · Kroger Specialty Pharmacy, Inc.
Key facts
| Event ID | 79748 |
|---|---|
| Recall numbers | D-0734-2018, D-0735-2018, D-0736-2018, D-0737-2018, D-0738-2018, D-0739-2018, D-0740-2018, D-0741-2018, D-0742-2018, D-0743-2018, D-0744-2018, D-0745-2018 and 55 more |
| Recalling firm | Kroger Specialty Pharmacy, Inc. |
| Product type | Drugs |
| Products | Albuterol 0.083% Inh Sol. 30 days supply, Rx Only, 39183, NDC 76204-0200-60, 30, Altera Handset NDC 83490-0678-05 56 days supply, Avonex 30 mcg/0.5 mL PFS Kit NDC 59627-0222-05 28 days supply, Azithromycin 250 mg tablet #18 TEV NDC 50111-0787-66 28 days supply, Bendeka 25 mg/mL 4 mL MDVPF NDC 63459-0348-04 28 days supply and 62 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Lack of Processing Controls. |
| Initiation date | Apr 3, 2018 |
| Report date | May 16, 2018 |
| Termination date | May 7, 2020 |
| City | Vicksburg |
| State | MS |
| Country | United States |
| FEI number | 3013456699 |
At a glance
- 10–99 Products in this recall
- None 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: