Stryker Instruments Div. of Stryker Corporation: Medical Device Recall in 2017 - (Recall #: Z-2071-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guidance system to enable intranasal and sinus computer-assisted surgery. The system is comprised of PROFESS Registration Stickers, a PROFESS Patient Tracker, and a PROFESS Adaptor Cable.

Product Classification:

Class II

Date Initiated: March 10, 2017

Date Posted: May 17, 2017

Recall Number: Z-2071-2017

Event ID: 77008

Reason for Recall:

Product shipped proximate to or past the expiration date listed on the product label.

Status: Terminated

Product Quantity: 65

Code Information:

Lot #202085 Stryker Product Number: 6001-420-000

Distribution Pattern:

US (nationwide) Distribution to the states of : CA, CT, GA, IL, IN, MA, MD, NC, OH, PA, TN, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated