DrKids Children's Cough & Chest Congestion DM — Class II drug recall D-1301-2019
Terminated recall by Unipharma, Llc., reported 2019-05-22, distributed nationwide. CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bac
| Recall number | D-1301-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Unipharma, Llc., Tamarac, FL, United States |
| Recall initiated | 2019-05-02 |
| Classified | 2019-05-23 |
| Reported by FDA | 2019-05-22 |
| Terminated | 2020-11-25 |
| Distributed | Nationwide (US) |
| Countries outside the US | VE |
| Quantity | 1,344 cartons |
| Reason classes | microbial contamination, cgmp |
| Pathogens | burkholderia |
| UPC / GTIN / UDI-DI | 00370302268010 |
| NDC | 70302-0013-20 |
| Lot numbers | 80054 |
| Expiration dates | 2020-10-31 |
Product
DrKids Children's Cough & Chest Congestion DM, Dextromethorphan HBr 5 mg Guaifenesin 100 mg Mixed Berry Flavor 20 Pre-measured Singe-Use 0.17 fl. oz. (5 mL), Manufactured in USA by: Unipharma, LLC. Tamarac, FL 33321, NDC 70302-013-20, UPC 370302268010
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-1301-2019. 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.