Neocis Inc.: Medical Device Recall in 2020 - (Recall #: Z-2637-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

DRW-0739-01: Gen 2 Posterior Chairside Splint LLUR (lower left-upper right) - Product Usage: intended to provide assistance in both the planning (pre-operative) and the surgical (intra-operative) phases of dental implantation surgery.

Product Classification:

Class II

Date Initiated: May 14, 2020

Date Posted: July 22, 2020

Recall Number: Z-2637-2020

Event ID: 85856

Reason for Recall:

The LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.

Status: Terminated

Product Quantity: 70 units

Code Information:

Work Order (lot): 1619 and 1620

Distribution Pattern:

US Nationwide distribution including in the states of AZ, CA, FL, NY, and NH

Voluntary or Mandated:

Voluntary: Firm initiated