Smith & Nephew, Inc.: Medical Device Recall in 2022 - (Recall #: Z-1418-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

(1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186. (2) Genesis II Non-Porous Tibial Baseplate Size 4 Left, Product #71420166.

Product Classification:

Class II

Date Initiated: June 27, 2022

Date Posted: July 27, 2022

Recall Number: Z-1418-2022

Event ID: 90547

Reason for Recall:

The product was mispackaged (swapped). The devices within the inner tray matches the inner tray but does not match the outer box label and the chart sticks.

Status: Completed

Product Quantity: 31 devices

Code Information:

Product #71420186 - Lot #21DM14954S, exp. October 2030, UDI #03596010206350. Product #71420166 - Lot #21FM13870A, exp. October 2030, UDI #03596010206268.

Distribution Pattern:

US Nationwide distribution in the states of AZ, CA, GA, KS, LA, MN, MI, MO, MS, NC, NJ, NY, OR, SC, TN, VA, WA, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated