READYPREP PVP — Class III drug recall D-0674-2025
Ongoing recall by Medline Industries, LP, reported 2025-10-01, distributed nationwide. Subpotent drug
| Recall number | D-0674-2025 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-08-19 |
| Classified | 2025-09-24 |
| Reported by FDA | 2025-10-01 |
| Distributed | Nationwide (US) |
| Quantity | 2,680 bottles |
| Reason classes | potency |
| NDC | 53329-0939, 53329-0939-04, 53329-0939-06, 53329-0939-08, 53329-0939-13, 53329-0939-23, 53329-0939-25, 53329-0939-69 |
| Lot numbers | 24EJA180 |
| Expiration dates | 2027-06-01 |
Product
READYPREP PVP, Povidone-Iodine 10% Solution, Topical Antiseptic, Not Sterile, 1 Gallon (3.78 L) per bottle, Manufactured in USA by Medline Industries, LP., Three Lakes Drive, Northfield, IL 60093, NDC 53329-939-25
Reason for recall
Subpotent drug
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-0674-2025. 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.