ROi CPS recalls a general surgery convenience kit (Item 880251013) containing 3M surgical drapes that were distributed but later recalled. No specific remedy is stated in the official notice.
Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.
ROi CPS has recalled a general surgery convenience kit (Item 880251013) that contains 3M surgical drapes. This recall was initiated because the drapes were distributed but later found to be problematic, though no specific remedy is stated in the official notice.
The recall involves surgical drapes that were distributed but later found to be problematic. However, the official notice does not specify the exact hazard mechanism or why the drapes were recalled.
Healthcare professionals using this surgical convenience kit are likely affected. Those who have the kit with the specified item number and lot numbers are at risk.
Check for the item number 880251013 and lot numbers 91465 (expiring 2/7/2024) or 92444 (expiring 5/5/2024) on the kit.
Look for the item number 880251013 and lot numbers 91465 or 92444 on the surgical convenience kit.
The official recall notice states that 3M surgical drapes were distributed but later found to be problematic, though the specific reason is not detailed.
The official notice does not specify a remedy, so no action is required beyond checking the kit details.
The official notice does not describe a specific hazard mechanism, so the risk level is unknown.
We’ve drafted a message you can send ROi CPS to request your refund or repair — edit it as you like.
Subject: Recall Z-0314-2023 — ROi CPS ROi CPS Hello, I own a ROi CPS that is covered by recall Z-0314-2023 from ROi CPS. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.