PDI Povidone-Iodine Prep Pad Large — Class II drug recall D-0759-2021
Terminated recall by Professional Disposables International, Inc, reported 2021-09-01, distributed nationwide. SubPotent: Out of Specification
| Recall number | D-0759-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Professional Disposables International, Inc, Woodcliff Lake, NJ, United States |
| Recall initiated | 2021-07-23 |
| Classified | 2021-08-20 |
| Reported by FDA | 2021-09-01 |
| Terminated | 2023-05-31 |
| Distributed | Nationwide (US) |
| Quantity | 1,982 cases |
| Reason classes | potency, specification failure |
| UPC / GTIN / UDI-DI | 00310819000154 |
| NDC | 10819-3883, 10819-3883-01, 10819-3883-03, 10819-3885, 10819-3885-01, 10819-3885-02 |
| Lot numbers | 11801215, 11801504, 11801717, 11900421, 11901076, 11901571, 12000388, 12001533, 12100459 |
| Expiration dates | 2021-08-22, 2021-11-06, 2021-12-07, 2022-04-04, 2022-08-29, 2022-11-19, 2023-03-13, 2023-07-28, 2024-03-31 |
Product
PDI Povidone-Iodine Prep Pad Large, 1 Prep Pad, Professional Disposable International, Inc., Orangeburg, NY 10962 -1376 USA Reorder No C12400 NDC 10819-3883-3, UPC (01)00310819000154
Reason for recall
SubPotent: Out of Specification
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-0759-2021. 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.