Panagel Hand Sanitizer — Class II drug recall D-0037-2021
Ongoing recall by Genesis Partnership Company SA, reported 2020-10-28, distributed nationwide. CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another
| Recall number | D-0037-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Genesis Partnership Company SA, Villa Nueva, N/A, Guatemala |
| Recall initiated | 2020-09-11 |
| Classified | 2020-10-19 |
| Reported by FDA | 2020-10-28 |
| Distributed | Nationwide (US) |
| Quantity | 33,480 bottles |
| Reason classes | potency, cgmp |
| UPC / GTIN / UDI-DI | 00378384000016 |
| NDC | 78384-0001-04 |
| Lot numbers | 072120 |
| Expiration dates | 2022-01-21 |
Product
Panagel Hand Sanitizer, 70% Alcohol,16 Fl. Oz. (472 mL) bottle, Made in Guatemala, Distributed by Central Med Distribution, 6100 Hollywood Blvd, Hollywood FL 33024, NDC 78384-001-04, UPC 378384000016.
Reason for recall
CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another hand sanitizer product with sub-potent ethanol levels.
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-0037-2021. 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.