Bioseal Corporation recalls custom surgical kits with expired Aplicare Providone Iodine Prep Pads. These kits may have incorrect expiration dates from Medline Industries' recall. Affected kits include specific models and lot numbers listed in the notice.
Custom surgical kits contain Aplicare Providone Iodine Prep Pads which were subsequently recalled by Medline Industries for in incorrect expiration date.
Bioseal Corporation is recalling custom surgical kits that contain Aplicare Providone Iodine Prep Pads with incorrect expiration dates. This recall follows Medline Industries' earlier recall of the same prep pads, which could lead to improper sterilization or infection risks if used.
The prep pads contain an incorrect expiration date, which could lead to improper sterilization or infection risks if used. This is a follow-up to Medline Industries' recall of the same prep pads for similar issues.
Healthcare professionals using these surgical kits are most at risk. Patients undergoing surgery with these kits may face infection risks due to expired prep pads.
Check for kits labeled with model numbers: Suture Removal Set (910-0002), Instrument Set (INST03/20), Suture Removal Set (SUT309/100), Incision & Drainage Tray (INC03/20), Suture Removal Set (SUT103/50), General Purpose Tray (GPT010/25), or General Purpose Tray (GPT002/50). Also check the lot numbers listed in the recall notice.
Look for specific model numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
The kits contain Aplicare Providone Iodine Prep Pads with incorrect expiration dates, which was previously recalled by Medline Industries.
Check for the specific model numbers and lot numbers listed in the recall notice, such as Suture Removal Set (910-0002) with lot numbers 400348, 400354, etc.
The recall notice does not specify a remedy, so contact Bioseal Corporation directly for guidance.
We’ve drafted a message you can send Bioseal to request your refund or repair — edit it as you like.
Subject: Recall Z-0085-2018 — Bioseal Bioseal Hello, I own a Bioseal that is covered by recall Z-0085-2018 from Bioseal. 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.
