FDA Drug recall D-0291-2019
SHEER DesenZ Desensitizing Treatment, Rx Only, Potassium Nitrate 12mg per film
- FDA Drug
- Class II
- terminated
- Published 2018-12-19
On 2018-12-19 the FDA classified a Class II recall of SHEER DesenZ Desensitizing Treatment, Rx Only, Potassium Nitrate 12mg per film by Cao Group, citing cGMP violations noted during the firm's most recent inspection.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0291-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-11-16 |
| Published | 2018-12-19 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Cao Group |
| Distribution | US |
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
cGMP violations noted during the firm's most recent inspection.
Identifiers
| upc | 872320000721 |
|---|---|
| code_info | Lot # 170626, EXP 6/26/2019; and 180131, EXP 01/31/2020 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0291-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.