Data Foundry

Drug recalls 2020

Ear Pain MD Pain Relief Drops with 4% Lidocaine — Class II drug recall D-1499-2020

Terminated recall by Eosera, Inc., reported 2020-08-19, distributed nationwide. cGMP Deviations.

Recall numberD-1499-2020
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmEosera, Inc., Fort Worth, TX, United States
Recall initiated2020-08-04
Classified2020-08-13
Reported by FDA2020-08-19
Terminated2021-09-10
DistributedNationwide (US)
Quantity125,874 bottles
Reason classescgmp
NDC72429-0072-02
Lot numbersP183017SEP, P183018, P192005, P193001, P193002, P193003, P193006, P193007, P193008, P193009, P193010, P193011, P193014JAN, P193053JUN, P193055, P193056, P193057, P193059, P193062, P193063, P193064, P193067FEB, P193068, P193087APR, P193088, P193089, P193091, P193097MAY, P203001, P203002, P203015, P203016, P203017JUL, P203024, P203030, P203033, P203040, P203044, P203047, P203057AUG and 3 more

Product

Ear Pain MD Pain Relief Drops with 4% Lidocaine (lidocaine HCl Monohydrate 4%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0072-2

Reason for recall

cGMP Deviations.

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-1499-2020. 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.