ROi CPS LLC recalls custom procedure packs with Clearlink Continu-Flo devices due to potential incorrect use during surgical procedures. Affected items include specific model numbers and lot numbers.
ROi CPS, LLC manufactured custom procedure packs using Clearlink Continu-Flo devices which were subsequently recalled by Baxter Healthcare Corporation.
ROi CPS LLC recalled custom procedure packs containing Clearlink Continu-Flo devices because they were manufactured with devices that could be used incorrectly during surgery. This recall affects specific model numbers and lot numbers listed in the product description.
The recalled devices were manufactured by ROi CPS LLC using Clearlink Continu-Flo products that could be used incorrectly during surgical procedures. This risk arises from potential misapplication of the devices in the operating room.
Healthcare professionals using these custom procedure packs during surgical procedures are most at risk. Patients undergoing surgery with these packs may face incorrect use of medical devices.
Check for product labels with model numbers like LD00200L-VAG DELIVERY MOTHER or GS00310C, and lot numbers such as 72700L or 74508L. These packs were sold in specific locations including Joplin and Lebanon.
Look for model numbers and lot numbers on the product labels to confirm if your item is affected.
ROi CPS LLC manufactured custom procedure packs using Clearlink Continu-Flo devices that could be used incorrectly during surgical procedures.
Affected items include model numbers like LD00200L-VAG DELIVERY MOTHER (lot 72700L, 74508L) and GS00310C (lot 72702C, 74406C).
Check for product labels with model numbers and lot numbers listed in the recall notice, such as LD00200L-VAG DELIVERY MOTHER or GS00310C with specific lot numbers.
We’ve drafted a message you can send ROi CPS to request your refund or repair — edit it as you like.
Subject: Recall Z-0918-2020 — ROi CPS ROi CPS Hello, I own a ROi CPS that is covered by recall Z-0918-2020 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.
