Zinc Oxide Paste 25% — Class III drug recall D-0695-2017
Terminated recall by Fagron, Inc, reported 2017-05-10, distributed nationwide. Labeling: Error on Declared Strength: Error is due to an incorrect value in the Drug Facts Panel. The correct
| Recall number | D-0695-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fagron, Inc, Saint Paul, MN, United States |
| Recall initiated | 2017-04-17 |
| Classified | 2017-05-03 |
| Reported by FDA | 2017-05-10 |
| Terminated | 2017-08-11 |
| Distributed | Nationwide (US) |
| Reason classes | labeling, potency |
| NDC | 51522-0694-05 |
| Lot numbers | 17C01-U07-036096 |
| Expiration dates | 2020-05-01 |
Product
Zinc Oxide Paste 25%, 500 g, For Prescription Compounding, Fagron Inc.2400 Pilot Knob Rd, St. Paul, MN 55120m NDC 51522-0694-5.
Reason for recall
Labeling: Error on Declared Strength: Error is due to an incorrect value in the Drug Facts Panel. The correct strength is displayed on the primary container.
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-0695-2017. 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.