ROi CPS recalls shoulder arthroscopy kits with 3M surgical drapes due to potential safety issues. Affected items include specific model numbers and lot dates.
Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.
ROi CPS is recalling shoulder arthroscopy surgical kits that contain 3M surgical drapes. This recall is due to the drapes being part of a previously recalled product line, though the specific hazard isn't detailed in the notice.
The recall involves surgical drapes that were previously part of a different product line. Without specific details on the hazard, it's unclear how the drapes could cause harm during surgery.
Orthopedic surgeons and medical facilities that use shoulder arthroscopy kits with the specified model number and lot dates are likely affected. Patients undergoing surgery with these kits may be at risk if the drapes are used improperly.
Check for the model number OR01103A and item number 880471001 on the kit. The lot number 92206 with an expiration date of January 26, 2024, is also associated with this recall.
Look for the model number OR01103A and item number 880471001 on the surgical kit.
The recall involves surgical drapes that were previously part of a different product line, but the specific hazard isn't detailed in the notice.
The official notice doesn't specify a remedy, so check with ROi CPS for further instructions.
The recall 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-0322-2023 — ROi CPS ROi CPS Hello, I own a ROi CPS that is covered by recall Z-0322-2023 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.
