Reported Sep 1, 2021 · Terminated

PDI Povidone-Iodine Swabstick (3's), 3 Swabsticks, 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 Povidone-Iodine Swabstick (3's), 3 Swabsticks, Professional Disposable International, Inc., Orangeburg, NY 10962 -1376 Reorder No S41125 NDC 10819-3885-2, UPC (01)00310819000185
Lot codes and dates
  • 172 of 172 codes

    • Lot #'s 11900761
    • EXP 2022-11-03
    • 11900917
    • EXP 2022-11-04
    • 11900918
    • EXP 2022-11-05
    • 11901008
    • EXP 2022-11-06
    • 11901009
    • EXP 2022-11-07
    • 11901124
    • EXP 2022-11-08
    • 11901125
    • EXP 2022-11-09
    • 11901126
    • EXP 2022-11-10
    • 11901127
    • EXP 2022-11-11
    • 11901179
    • EXP 2022-11-12
    • 11901180
    • EXP 2022-11-13
    • 11901247
    • EXP 2022-11-14
    • 11901248
    • EXP 2022-11-15
    • 11901388
    • EXP 2022-11-16
    • 11901389
    • EXP 2022-11-17
    • 11901390
    • EXP 2022-11-18
    • 11901419
    • EXP 2022-11-19
    • 11901420
    • EXP 2022-11-20
    • 11901480
    • EXP 2022-11-21
    • 11901558
    • EXP 2022-11-22
    • 11901590
    • EXP 2022-11-23
    • 11901591
    • EXP 2022-11-24
    • 11901592
    • EXP 2022-11-25
    • 11901691
    • EXP 2022-11-26
    • 11901692
    • EXP 2022-11-27
    • 12000054
    • EXP 2022-11-28
    • 12000055
    • EXP 2022-11-29
    • 12000116
    • EXP 2022-11-30
    • 12000117
    • EXP 2022-12-01
    • 12000172
    • EXP 2022-12-02
Amount recalled
51,926 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, 7:20 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.