Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol — Class III drug recall D-0072-2018
Terminated recall by Dr. Reddy's Laboratories, Inc., reported 2017-11-15, distributed nationwide. Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the secondary packaging doesnt match the lo
| Recall number | D-0072-2018 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dr. Reddy's Laboratories, Inc., Princeton, NJ, United States |
| Recall initiated | 2017-10-30 |
| Classified | 2017-11-07 |
| Reported by FDA | 2017-11-15 |
| Terminated | 2020-03-20 |
| Distributed | Nationwide (US) |
| Quantity | 23,402 cases |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00849648000023 |
| Lot numbers | 2462100R, 2583800R |
| Expiration dates | 2018-09, 2018-11 |
Product
Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube, Distributed by: Ducere Pharma, LLC New Hope, PA 18938 USA --- UPC 849648000023
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the secondary packaging doesnt match the lot number printed on the bottle
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-0072-2018. 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.