Data Foundry

Drug recalls 2020

New! Rompe Pecho MAX Multi Symptoms — Class II drug recall D-0847-2020

Terminated recall by Efficient Laboratories, Inc., reported 2020-02-19, distributed nationwide. Microbial Contamination of Non-Sterile Products

Recall numberD-0847-2020
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmEfficient Laboratories, Inc., Miami, FL, United States
Recall initiated2020-01-31
Classified2020-02-14
Reported by FDA2020-02-19
Terminated2020-10-22
DistributedNationwide (US)
Quantity4,080
Reason classesmicrobial contamination, sterility
UPC / GTIN / UDI-DI00000856003095
Lot numbers19B42
Expiration dates2022-02-20

Product

New! Rompe Pecho MAX Multi Symptoms, 8 FL. Oz (237 mL) bottle, Distributed by: Efficient Laboratories, Inc. Miami, FL 33166. UPC 0 00856 00309 5

Reason for recall

Microbial Contamination of Non-Sterile Products

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-0847-2020. 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.