ROi CPS recalls a neuro surgery convenience kit with 3M surgical drapes due to potential minor neuro risks. Affected items include specific lot numbers and expiration dates.
Surgical convenience kits were distributed containing 3M surgical drapes which were subsequently recalled.
ROi CPS is recalling a neuro surgery convenience kit that contains 3M surgical drapes. This recall is due to a potential minor neurological risk associated with the drapes.
The surgical drapes in the kit could pose a minor neurological risk if they are used incorrectly during neurosurgery. This risk is not severe but requires careful handling to avoid potential complications.
Healthcare professionals using the neuro surgery convenience kit are most likely affected. Patients or others using the kit during surgery may be at risk if the drapes are used improperly.
Check for the item number 880135030 and lot numbers 91012 (exp 9/28/2023), 91752 (exp 1/29/2024), or 92497 (exp 2/14/2024). The kit was sold with the UDI/DI 10194717111306.
Verify the item number and lot numbers listed in the recall notice to confirm if your kit is affected.
The recall is for a potential minor neurological risk, not a serious hazard. The risk is low and requires careful use.
The recall does not specify a remedy, so check the product details to see if your kit is affected.
Look for the item number 880135030 and lot numbers 91012, 91752, or 92497 with the specified expiration dates.
We’ve drafted a message you can send ROi CPS to request your refund or repair — edit it as you like.
Subject: Recall Z-0311-2023 — ROi CPS ROi CPS Hello, I own a ROi CPS that is covered by recall Z-0311-2023 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.