Drug recall
Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ (355 mL) bottles…
FDA recall event 77450 · Class III · L. Perrigo Company
Key facts
| Event ID | 77450 |
|---|---|
| Recall numbers | D-0925-2017 |
| Recalling firm | L. Perrigo Company |
| Product type | Drugs |
| Products | Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ (355 mL) bottles connected by one paper sleeve, TOTAL 24 FL OZ (1.5 pt)(710 mL), OTC, Distributed by: Walgreen… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the batch… |
| Initiation date | Jun 5, 2017 |
| Report date | Jul 5, 2017 |
| Termination date | Dec 7, 2017 |
| 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: