Reported Sep 1, 2021 · Terminated
PDI Povidone-Iodine Prep Pad MEDIUM, 1 Prep Pad [2.0x2.5 in (5.1x6.4 cm)], Professional Disposables International Inc.,…
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 Prep Pad MEDIUM, 1 Prep Pad [2.0x2.5 in (5.1x6.4 cm)], Professional Disposables International Inc., Orangeburg, NY 10962-1376 Reorder No. B40600; UPC (01)00310819000147, NDC 10819-3883-1,
- Lot codes and dates
163 of 163 codes
Lot #'s EXP date 118009772021-07-3111800978 2021-08-0211800979 2021-08-0411801123 2021-08-0611801124 2021-08-0911801125 2021-08-1511801126 2021-08-1611801228 2021-08-2811801230 2021-09-1111801231 2021-09-1311801232 2021-09-1811801234 2021-10-2511801417 2021-10-2811801418 2021-11-0111801419 2021-11-0711801420 2021-11-1511801421 2021-11-2011801709 2021-11-2911801710 2021-12-0411900195 2022-02-1911900196 2022-02-2111900197 2022-02-2511900370 2022-04-0111900372 2022-04-0311900371 2022-04-0511900647 2022-05-0411900623 2022-05-2111900624 2022-05-2411900646 2022-05-2911900967 2022-08-1311900968 2022-08-2611900969 2022-08-2811901043 2022-09-1111901044 2022-09-1811901318 2022-10-0311901330 2022-10-0811901331 2022-10-1611901446 2022-10-2811901447 2022-11-1911901448 2022-12-1911901739 2023-01-0211901752 2023-01-0912000045 2023-01-1412000048 2023-01-1812000046 2023-01-2112000047 2023-01-2412000333 2023-01-2512000675 2023-02-1612000334 2023-02-2712000335 2023-02-2712000336 2023-02-2812000676 2023-03-1612000815 2023-03-2912000816 2023-05-0512000914 2023-05-1312000915 2023-05-1812000951 2023-05-2212000950 2023-06-0112001366 2023-08-12
- Amount recalled
- 53588 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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