DrKids Children's Allergy Relief Diphenhydramine HCl 12 — Class II drug recall D-1632-2019
Terminated recall by Unipharma, Llc., reported 2019-08-14, distributed nationwide. CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bac
| Recall number | D-1632-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Unipharma, Llc., Tamarac, FL, United States |
| Recall initiated | 2019-07-15 |
| Classified | 2019-08-08 |
| Reported by FDA | 2019-08-14 |
| Terminated | 2020-06-05 |
| Distributed | Nationwide (US) |
| Quantity | 432 cartons |
| Reason classes | microbial contamination, cgmp |
| Pathogens | burkholderia |
| UPC / GTIN / UDI-DI | 00370302255010 |
| Lot numbers | 90003 |
| Expiration dates | 2021-01-31 |
Product
DrKids Children's Allergy Relief Diphenhydramine HCl 12.5 mg/5 mL Antihistamine, Mixed berry Flavor, 20 Pre-measured Single-Use vials per Carton, Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, UPC 370302255010
Reason for recall
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
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-1632-2019. 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.