Allergy ALLER-FEX — Class II drug recall D-0905-2023
Terminated recall by L. Perrigo Company, reported 2023-07-19, distributed nationwide. Failed Impurities/Degradation Specifications
| Recall number | D-0905-2023 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | L. Perrigo Company, Allegan, MI, United States |
| Recall initiated | 2023-02-09 |
| Classified | 2023-07-11 |
| Reported by FDA | 2023-07-19 |
| Terminated | 2023-09-11 |
| Distributed | Nationwide (US) |
| Quantity | 360,184 |
| Reason classes | specification failure |
| NDC | 63981-0847, 63981-0847-48 |
| Lot numbers | 01/24, 04/24, 11/23, 12/23, 2DV1487, 2DV1870, 2DV1871, 2DV1873, 2DV2000, 2EV1666, 2EV1667, 2EV1668, 2EV1670, 2EV1671, 2EV1672, 2EV1674, 2EV1676, 2EV1677, 2EV1678, 2FV1764, 2FV1765, 2FV1766, 2GV1579, 2GV1937, 2GV1941, 2GV1942, 2GV2132, 2GV2157, 2HV1886, 2HV1997, 2HV2017, 2HV2019, 2HV2047, 2HV2679, 2LV1573, 2MV1314, V02/24 |
Product
Allergy ALLER-FEX, Fexofenadine Hydrochloride Tablets, 180 mg, 180-count cartons, Packaged by: Perrigo, 515 Eastern Ave., Allegan, MI 49010 USA. NDC 63981-847-48
Reason for recall
Failed Impurities/Degradation Specifications
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-0905-2023. 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.