Reported Sep 1, 2021 · Terminated

PDI Povidine Iodine Swabstick (1's), 1 swabstick, Professional Disposable International, Inc. Orangeburg, NY 10962…

Professional Disposables International, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Professional Disposables International, Inc · 400 Chestnut Ridge Rd · Woodcliff Lake, NJ · 07677-7604

Is this the product you have?

  • 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.
Lot codes and dates
  • 132 of 132 codes

    • Lot #'s 11900790
    • EXP 2021-07-25
    • 11900919
    • EXP 2021-07-28
    • 11900920
    • EXP 2021-08-12
    • 11900921
    • EXP 2021-08-15
    • 11901106
    • EXP 2021-08-27
    • 11901107
    • EXP 2021-08-30
    • 11901128
    • EXP 2021-09-05
    • 11901129
    • EXP 2021-09-12
    • 11901249
    • EXP 2021-09-25
    • 11901250
    • EXP 2021-10-17
    • 11901391
    • EXP 2021-10-19
    • 11901392
    • EXP 2021-10-22
    • 11901438
    • EXP 2021-10-24
    • 11901439
    • EXP 2021-10-08
    • 11901457
    • EXP 2021-11-07
    • 11901541
    • EXP 2021-11-18
    • 11901603
    • EXP 2021-11-19
    • 11901604
    • EXP 2021-12-19
    • 11901669
    • EXP 2021-12-19
    • 11901670
    • EXP 2021-11-16
    • 11901702
    • EXP 2021-12-02
    • 11901703
    • EXP 2021-12-14
    • 12000082
    • EXP 2021-12-19
    • 12000083
    • EXP 2022-01-24
    • 12000118
    • EXP 2022-01-03
    • 12000119
    • EXP 2022-01-30
    • 12000249
    • EXP 2022-01-10
    • 12000250
    • EXP 2022-01-10
    • 12000348
    • EXP 2022-02-13
    • 12000349
    • EXP 2022-02-28
Amount recalled
41,105 cases

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide

Why it was recalled

SubPotent: Out of Specification

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated May 31, 2023 · Data as of Sep 19, 7:23 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.