Ceterix recalls CTX-C001 orthopedic suture cutters due to potential higher cut force. Affected items may cause suture damage during surgery. Contact for replacement.
Possible nonconforming blades may result in a higher than specified cut force required to cut the suture.
Ceterix is recalling its CTX-C001 disposable knot pushers and suture cutters for orthopedic surgery use. The recall is because these tools might require more force to cut sutures than intended, which could lead to complications during procedures.
The blades in the CTX-C001 model may require more force to cut sutures than designed. This could cause the suture to tear or become damaged during surgery, potentially leading to complications for the patient.
Orthopedic surgeons and surgical teams using the CTX-C001 model during arthroscopic procedures are most at risk. Patients undergoing surgery with these tools may experience complications if the cut force is higher than intended.
Check for the model number CTX-C001 on the product. The recall covers items sold with lot number M180018. This product is used in orthopedic arthroscopic surgeries.
Look for the model number CTX-C001 on the disposable knot pusher or suture cutter.
The recall states that the blades may require higher cut force than intended, which could cause suture damage during surgery. However, the remedy is not specified in the record.
Check for the model number CTX-C001 and lot number M180018 on the product. This is an orthopedic arthroscopic accessory.
The recall record does not specify a remedy, so no action is required based on the information provided.
We’ve drafted a message you can send Ceterix to request your refund or repair — edit it as you like.
Subject: Recall Z-2945-2018 — Ceterix Ceterix Hello, I own a Ceterix that is covered by recall Z-2945-2018 from Ceterix. 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.
