Povidone Iodine — Class II drug recall D-0152-2020
Terminated recall by Avella of Deer Valley, Inc. Store 38, reported 2019-10-30, distributed nationwide. Lack of sterility assurance.
| Recall number | D-0152-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Recalling firm | Avella of Deer Valley, Inc. Store 38, Phoenix, AZ, United States |
| Recall initiated | 2019-09-18 |
| Classified | 2019-10-18 |
| Reported by FDA | 2019-10-30 |
| Terminated | 2019-12-04 |
| Distributed | Nationwide (US) |
| Quantity | 808 droptainers |
| Reason classes | sterility |
| NDC | 42852-0006-20 |
| Expiration dates | 2019-11-03 |
Product
Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416 N. 19th Ave., Phoenix, AZ 85085. NDC 42852-006-20
Reason for recall
Lack of sterility assurance.
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-0152-2020. 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.