Data Foundry

Drug recalls 2024

IBU Ibuprofen Tablets — Class II drug recall D-0644-2024

Ongoing recall by Dr. Reddy's Laboratories, Inc., reported 2024-09-04, distributed nationwide. Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively,

Recall numberD-0644-2024
Product typeDrug
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmDr. Reddy's Laboratories, Inc., Princeton, NJ, United States
Recall initiated2024-08-06
Classified2024-08-26
Reported by FDA2024-09-04
DistributedNationwide (US)
Quantity103,298 bottles
Reason classesspecification failure
NDC55111-0682, 55111-0682-01, 55111-0682-05, 55111-0682-09, 55111-0683, 55111-0683-01, 55111-0683-05, 55111-0683-09, 55111-0683-30, 55111-0683-50, 55111-0684, 55111-0684-01, 55111-0684-05, 55111-0684-09, 55111-0684-30, 55111-0684-50, 55111-0684-60
Lot numbersC2207525, C2207526, C2210751, C2210752, C2212765, C2212766, C2212902, C2301027, C2301063, C2301187, C2301188, C2301247, C2301356, C2301388, C2301478, C2301494, C2301617, C2303381, C2303432, C2303565, C2303630, C2303643, C2303710, C2303806, C2303879, C2303895, C2303963, C2304130, C2304163, C2304263, C2304264, C2304427
Expiration dates2026-05-31, 2026-09-30, 2026-11-30, 2026-12-31, 2027-01-31, 2027-02-28, 2027-03-31

Product

IBU Ibuprofen Tablets, USP, 800 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-684-01 - 100 Tablets per bottle, b)NDC 55111-684-05 - 500 Tablets per bottle.

Reason for recall

Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.

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-0644-2024. 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.