Data Foundry

Drug recalls 2021

PDI Povidine Iodine Swabstick — Class II drug recall D-0760-2021

Terminated recall by Professional Disposables International, Inc, reported 2021-09-01, distributed nationwide. SubPotent: Out of Specification

Recall numberD-0760-2021
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmProfessional Disposables International, Inc, Woodcliff Lake, NJ, United States
Recall initiated2021-07-23
Classified2021-08-20
Reported by FDA2021-09-01
Terminated2023-05-31
DistributedNationwide (US)
Quantity41,105 cases
Reason classespotency, specification failure
UPC / GTIN / UDI-DI00310819000178
NDC10819-3883, 10819-3883-01, 10819-3883-03, 10819-3885, 10819-3885-01, 10819-3885-02
Lot numbers11900790, 11900919, 11900920, 11900921, 11901106, 11901107, 11901128, 11901129, 11901249, 11901250, 11901391, 11901392, 11901438, 11901439, 11901457, 11901541, 11901603, 11901604, 11901669, 11901670, 11901702, 11901703, 12000082, 12000083, 12000118, 12000119, 12000249, 12000250, 12000348, 12000349, 12000398, 12000456, 12000457, 12000683, 12000684, 12000685, 12000922, 12000923, 12000927, 12000989 and 26 more
Expiration dates2021-07-25, 2021-07-28, 2021-08-12, 2021-08-15, 2021-08-27, 2021-08-30, 2021-09-05, 2021-09-12, 2021-09-25, 2021-10-08, 2021-10-17, 2021-10-19, 2021-10-22, 2021-10-24, 2021-11-07, 2021-11-16, 2021-11-18, 2021-11-19, 2021-12-02, 2021-12-14, 2021-12-19, 2022-01-03, 2022-01-10, 2022-01-24, 2022-01-30 and 26 more

Product

PDI Povidine Iodine Swabstick (1's), 1 swabstick, Professional Disposable International, Inc. Orangeburg, NY 10962 -1376 Reorder No S41350 NDC 10819-3885-1, UPC (01)00310819000178.

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-0760-2021. 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.