Lidothol Patch — Class II drug recall D-1390-2020
Terminated recall by Preferred Pharmaceuticals, Inc., reported 2020-07-22, distributed nationwide. CGMP Deviations: Contract Manufacturing Organization (CMO) misplaced/lost batch records and test results for t
| Recall number | D-1390-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Preferred Pharmaceuticals, Inc., Anaheim, CA, United States |
| Recall initiated | 2020-07-01 |
| Classified | 2020-07-15 |
| Reported by FDA | 2020-07-22 |
| Terminated | 2024-04-17 |
| Distributed | Nationwide (US) |
| Reason classes | cgmp |
| NDC | 53225-1025-01, 68788-7405-01 |
| Lot numbers | A0419M, G0519G, H0218Z, H1518J, I2018L, J2918C, L1018Q |
| Expiration dates | 2021-05-31 |
Product
Lidothol Patch, Lidocaine 4.5% & Menthol 5%, In each patch: lidocaine 4.5% topical anesthetic, menthol 5% topical analgesic, Pkg Size 15 patches per box, Insurance NDC: 53225-1025-01, Mfg: Terrain Pharmaceuticals; Reno, NV, Prod # (NDC): 68788-7405-01, Preferred Pharmaceuticals, Inc., The Physicians Solutions.
Reason for recall
CGMP Deviations: Contract Manufacturing Organization (CMO) misplaced/lost batch records and test results for the recalled batch.
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-1390-2020. 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.