Stryker GmbH: Medical Device Recall in 2025 - (Recall #: Z-1620-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;

Product Classification:

Class II

Date Initiated: March 28, 2025

Date Posted: April 23, 2025

Recall Number: Z-1620-2025

Event ID: 96555

Reason for Recall:

The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.

Status: Ongoing

Product Quantity: 1588 units

Code Information:

Catalog number/REF: 2351-3080S; UDI-DI: 07613327361797; Lot #: KU155697, KU155698, KU155699, KU155700, KU155701, KU155702, KU155703, KU155704, KU155705, KU155706, KU155707, KU155708, KU155709, KU155710, KU155711, KU155712.

Distribution Pattern:

US Nationwide distribution in the states of CA, GA, IL, KY, MA, MD, NY, OH, TN, TX, WV.

Voluntary or Mandated:

Voluntary: Firm initiated