Data Foundry

Drug recalls 2023

Lidocaine Patch 5% — Class III drug recall D-0556-2023

Ongoing recall by Bryant Ranch Prepack, Inc., reported 2023-05-10, distributed nationwide. Labeling: Typographical error on the upper left-hand side of the box and individual patch label that has the i

Recall numberD-0556-2023
Product typeDrug
ClassificationClass III
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBryant Ranch Prepack, Inc., Burbank, CA, United States
Recall initiated2023-04-20
Classified2023-04-28
Reported by FDA2023-05-10
DistributedNationwide (US)
Quantity403 boxes
Reason classeslabeling
NDC63629-8755, 63629-8755-01, 63629-8755-02, 63629-8755-20
Lot numbers204550, 204555, 204599, 204601, 204603, 204604, 204832, 204871, 204996, 205127, 205324, 205494, 205611, 205612, 205615, 205616, 206232, 208295, 208445, 208608, 208609, 208749, 208975, 209101, 209102, 209106, 209211, 209212, 209548, 209624, 209706, 209779, 209839
Expiration dates2024-09-30, 2024-10-31, 2024-11-30, 2024-12-31

Product

Lidocaine Patch 5%, 1 patch (63629-8755-20) packaged in 30-count patches per carton (63629-8755-1), Rx only, each patch contains: 700 mg (50mg per gram adhesive) in an aqueous base, Manufactured by: Actavis Laboratories UT, Inc., Relabeled by: Bryant Ranch Prepack, Inc. Burbank, CA 91504 USA

Reason for recall

Labeling: Typographical error on the upper left-hand side of the box and individual patch label that has the incorrect dosage form stating, each tablet contains instead of each adhesive patch contains.

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-0556-2023. 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.