Arthrex, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2918-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Arthrex Suture Washer

Product Classification:

Class III

Date Initiated: August 12, 2016

Date Posted: October 12, 2016

Recall Number: Z-2918-2016

Event ID: 75050

Reason for Recall:

The device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package.

Status: Terminated

Product Quantity: 45 devices

Code Information:

Unique Device Identifier (UDI): 00888867118607; Catalog # AR-7000-18T; Batch #10028617.

Distribution Pattern:

OR, NY, MN, KY, CA, ID, CO, MA, and FL. Thailand.

Voluntary or Mandated:

Voluntary: Firm initiated