Stryker GmbH: Medical Device Recall in 2018 - (Recall #: Z-2393-2018)

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:

Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S

Product Classification:

Class II

Date Initiated: April 27, 2018

Date Posted: July 18, 2018

Recall Number: Z-2393-2018

Event ID: 80131

Reason for Recall:

The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.

Status: Terminated

Product Quantity: 12

Code Information:

GTIN 04546540197771; Lot code: K074846

Distribution Pattern:

The products were distributed to the following US states: AL, Co, FL, KY, NC, TN, UT, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated