Data Foundry

Drug recalls 2017

Ibuprofen Tablets — Class II drug recall D-1055-2017

Terminated recall by Time-Cap Laboratories, Inc., reported 2017-08-09, distributed nationwide. Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles were found to contain some Ibuprof

Recall numberD-1055-2017
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTime-Cap Laboratories, Inc., Farmingdale, NY, United States
Recall initiated2017-06-16
Classified2017-08-03
Reported by FDA2017-08-09
Terminated2020-05-29
DistributedNationwide (US)
Quantity1,980 bottles
NDC49483-0602, 49483-0602-01, 49483-0602-50, 49483-0603, 49483-0603-01, 49483-0603-03, 49483-0603-05, 49483-0603-50, 49483-0604, 49483-0604-01, 49483-0604-03, 49483-0604-05, 49483-0604-50
Lot numbersHN7003

Product

Ibuprofen Tablets, USP 600 mg, 500-count bottle (Capsule Shaped), Rx only, Manufactured for: Time Cap Labs, Inc., 7 Michael Avenue Farmingdale, NJ 11735, USA, Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83 Verna Indl. Estate, Verna, Goa-403 722, India, NDC 49483-603-50

Reason for recall

Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles were found to contain some Ibuprofen Tablets USP 800 mg.

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-1055-2017. 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.