PDI recalls large prep pads due to subpotent quality issues. These pads may not meet required iodine levels, potentially affecting disinfection effectiveness. Consumers should check lot numbers and expiration dates.
SubPotent: Out of Specification
Professional Disposables International (PDI) is recalling large povidone-iodine prep pads because they may have insufficient iodine levels. This could reduce their effectiveness as a disinfectant, especially in medical settings where proper sterilization is critical.
The prep pads have been found to be 'subpotent,' meaning they contain less active iodine than specified. This could lead to reduced disinfection effectiveness, potentially increasing infection risk during medical procedures. However, the hazard is not severe enough to cause immediate injury or death.
Healthcare professionals and medical facilities using these prep pads for surgical procedures or wound care are most at risk. Consumers who purchased these pads for home medical use may also be affected.
Check for lot numbers on the packaging: 11801215 (exp 2021-08-22), 11801504 (exp 2021-11-06), 11801717 (exp 2021-12-07), 11900421 (exp 2022-04-04), 11901076 (exp 2022-08-29), 11901571 (exp 2022-11-19), 12000388 (exp 2023-03-13), 12001533 (exp 2023-07-28), or 12100459 (exp 2024-03-31).
Look for lot numbers on the packaging: 11801215, 11801504, 11801717, 11900421, 11901076, 11901571, 12000388, 12001533, or 12100459.
The product was found to be 'subpotent,' meaning it contains less active iodine than specified, which could reduce its effectiveness as a disinfectant.
Check the lot number on the packaging to see if it matches the recalled lots listed. If it does, contact PDI for further instructions.
The recall is for reduced disinfection effectiveness, not a direct injury hazard. However, using ineffective disinfectants could increase infection risk in medical procedures.
We’ve drafted a message you can send PDI to request your refund or repair — edit it as you like.
Subject: Recall D-0759-2021 — PDI PDI Hello, I own a PDI that is covered by recall D-0759-2021 from PDI. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
