FDA Drug recall D-216-2013
PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel caps 20 count bliste…
- FDA Drug
- Class III
- terminated
- Published 2013-04-03
On 2013-04-03 the FDA classified a Class III recall of PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel caps 20 count bliste… by L Perrigo, citing subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-216-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-02-18 |
| Published | 2013-04-03 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | L Perrigo |
| Distribution | AR |
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
Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
Identifiers
| code_info | 2 AE1549 Exp. 02/13 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-216-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.