Ethicon recalls 5mm Endopath Xcel surgical devices with Optiview Technology due to potential surgery prolongation from insufficient lubrication. This may rarely cause minor particle introduction during repeated use.
Use of the product with insufficient lubrication may prolong surgery due to trocar replacement. In addition, insufficient lubrication could result in a remote chance of introducing a minute particle if repeated insertions of the obturator or laparoscopic device damage the seal.
Ethicon is recalling certain 5mm Endopath Xcel surgical devices with Optiview Technology. Insufficient lubrication during use could prolong surgery and rarely introduce tiny particles if the device is repeatedly inserted.
Insufficient lubrication during surgery may cause the trocar to need replacement, prolonging the procedure. Repeated insertions could rarely introduce tiny particles if the device's seal is damaged.
Surgical teams using the recalled 5mm Endopath Xcel devices with Optiview Technology. The risk is lowest for procedures where lubrication is consistently maintained.
Check for the model number 2CB5LT on the device. The product was sold with lot numbers starting with P4T or R400.
Look for the model number 2CB5LT on the device to confirm if it's recalled.
Yes, the recall is for when lubrication is insufficient during use, not for normal proper use.
Check for the model number 2CB5LT and lot numbers starting with P4T or R400 as listed in the recall.
The recall does not specify a remedy, so contact Ethicon directly for guidance.
We’ve drafted a message you can send Ethicon to request your refund or repair — edit it as you like.
Subject: Recall Z-1888-2018 — Ethicon Ethicon Hello, I own a Ethicon that is covered by recall Z-1888-2018 from Ethicon. 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.