Reported Feb 7, 2018 · Terminated

Aplicare Povidone-Iodine Prep Pad, Antiseptic, Sterile Solution, Active Ingredient: Povidone-iodine USP 10%. Aplicare,…

Medline Industries 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: Medline Industries Inc · Three Lakes Drive · Northfield, IL · 60093

Is this the product you have?

  • Aplicare Povidone-Iodine Prep Pad, Antiseptic, Sterile Solution
  • Active IngredientPovidone-iodine USP 10%. Aplicare, INC., Meriden, CT 06450 USA
  • NDC52380-0111-1
Lot codes and dates
  • Part # P-1001
  • Lots
    • 58471
    • 59003
    • 59723
    • 60373
    • 60807
    • 61187
    • 61523
    • 61998
    • 63974
    • 64701
    • 65864 Part #
  • P-1001-8S Lots
    • 58368
    • 58371
    • 58472
    • 58499
    • 58686
    • 58687
    • 58688
    • 58816
    • 58817
    • 58818
    • 59002
    • 59004
    • 59333
    • 59334
    • 59335
    • 59574
    • 59724
    • 59725
    • 60157
    • 60237
    • 60374
    • 60375
    • 60507
    • 60586
    • 61101
    • 61368
    • 61427
    • 61618
    • 61750
    • 61751
    • 61999
    • 62067
    • 62224
    • 62226
    • 62557
    • 62558
    • 62954
    • 62955
    • 63441
    • 63442
    • 63443
    • 63507
    • 63508
    • 64002
    • 64129
    • 64243
    • 64245
    • 64592
    • 64840
    • 65081
    • 65327
    • 65583
    • 65681
    • 65882
    • 66026
    • 66040
    • 66110
    • 66193
    • Part #
  • P-1011 Lots
    • 66549
    • 66916 Part #
  • P-1011-8S Lots
    • 66404
    • 66580
    • 66622
    • 66709
    • 66856
Amount recalled
11,750 cases

This recall covers 68 products

The agency filed one notice per product. You are reading one of them; the other 67 are below.

55 more are in the archive.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

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 Aug 28, 2023 · Data as of Sep 19, 5:53 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.