PE Daytime Cold/Flu LiqGel — Class III drug recall D-216-2013
Terminated recall by L. Perrigo Co., reported 2013-04-03, distributed in AR. Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
| Recall number | D-216-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | L. Perrigo Co., Allegan, MI, United States |
| Recall initiated | 2013-02-18 |
| Classified | 2013-03-22 |
| Reported by FDA | 2013-04-03 |
| Terminated | 2013-09-12 |
| Distributed | AR |
| Quantity | 60,048 blister |
| Reason classes | potency |
Product
PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel caps 20 count blister pack, Distributed By: Wal-Mat Stores Inc., Bentonville, AR, 72716
Reason for recall
Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
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-216-2013. 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.