CLASS II Drug recall · Reported 1 Sep 2021 · FDA Enforcement Report

PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabstick recalled

Professional Disposables International is recalling PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabstick, (1's), Step 1, packaged as a), distributed nationwide in the US. The recall was initiated on 23 Jul 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSKU S23125 Lot #'s 11900971, 11901517, 11901756, 12000199, 12000286, 12000459, 12000686, 12000751, 12001009, 12001316, 12001795, 12001809, 12001862, 12001863, 12002140, 12002141, 12100392 and 12100393
Quantity recalled11,039 cases

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0764-2021
FDA event ID
88326
Recalling firm
Professional Disposables International, Woodcliff Lake, NJ
Classification
Class II
Status
Terminated
Recall initiated
23 Jul 2021
FDA classified
20 Aug 2021
Reported
1 Sep 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

23 Jul 2021Recall initiated by company
20 Aug 2021Classified by FDA+28 days
1 Sep 2021Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

SubPotent: Out of Specification

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

PDI Duo-Swab Povidone-Iodine Cleansing Scrub Swabstick, (1's), Step 1, packaged as a) Step 1 Scrub, 1 Swabstick, NDC 10819-3891-1, b) Step 2 Prep, 1 Swabstick, NDC 10819-3890-1, Professional Disposable International, Inc., Orangeburg, NY 10962 -1376 Reorder No S23125, UPC (01)00318019000161

Where it was distributed

Distributed Nationwide in the US

Nationwide

Questions about this recall

Why was it recalled?

SubPotent: Out of Specification

Which lots are affected?

SKU S23125 Lot #'s 11900971, 11901517, 11901756, 12000199, 12000286, 12000459, 12000686, 12000751, 12001009, 12001316, 12001795, 12001809, 12001862, 12001863, 12002140, 12002141, 12100392 and 12100393

Where was it sold?

Distributed Nationwide in the US

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

6 other products · FDA event 88326

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