Drug recall
Loratadine orally disintegrating tablets, 10 mg, OTC; The product was distributed under the following labels…
FDA recall event 56594 · Class III · L. Perrigo Co.
Key facts
| Event ID | 56594 |
|---|---|
| Recall numbers | D-805-2010 |
| Recalling firm | L. Perrigo Co. |
| Product type | Drugs |
| Products | Loratadine orally disintegrating tablets, 10 mg, OTC; The product was distributed under the following labels: 1) CareOne Allergy Relief, i) 10 Tablets Count Box, NDC 41520-311-52, UPC 3 41520 31346 2… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent; 6 month stability |
| Initiation date | Jun 16, 2010 |
| Termination date | Oct 13, 2010 |
| 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