Ethicon Endo-Surgery Inc: Medical Device Recall in 2018 - (Recall #: Z-1887-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

5mm Endopath Xcel with Optiview Technology, Bladeless Trocar with Stability Sleeve, 5mm, 150mm shaft length, 2B5XT

Product Classification:

Class II

Date Initiated: March 26, 2018

Date Posted: May 23, 2018

Recall Number: Z-1887-2018

Event ID: 79801

Reason for Recall:

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.

Status: Terminated

Product Quantity: 1500

Code Information:

Lots P4TD1E R4001U R4052P

Distribution Pattern:

Nationwide domestic distribution, including PR. International distribution to Saudi Arabia, United Arab Emirates, Belgium, Singapore, Taiwan, South Korea, Canada, Chile, Mexico, Japan, and Argentina.

Voluntary or Mandated:

Voluntary: Firm initiated