SHEER DesenZ Desensitizing Treatment — Class II drug recall D-0291-2019
Terminated recall by CAO Group, Inc., reported 2018-12-19, distributed nationwide. cGMP violations noted during the firm's most recent inspection.
| Recall number | D-0291-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CAO Group, Inc., West Jordan, UT, United States |
| Recall initiated | 2018-11-16 |
| Classified | 2018-12-11 |
| Reported by FDA | 2018-12-19 |
| Terminated | 2020-02-27 |
| Distributed | Nationwide (US) |
| Quantity | 71 cartons |
| Reason classes | cgmp |
| UPC / GTIN / UDI-DI | 00872320000721 |
| Lot numbers | 170626, 180131 |
| Expiration dates | 2019-06-26, 2020-01-31 |
Product
SHEER DesenZ Desensitizing Treatment, Rx Only, Potassium Nitrate 12mg per film. CAO GROUP, INC, 4628 West Skyhawk Drive West Jordan, UT 84084. UPC: 8 72320 00072 1 NDC 1406000304
Reason for recall
cGMP violations noted during the firm's most recent inspection.
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-0291-2019. 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.