Stryker Instruments Div. of Stryker Corporation: Medical Device Recall in 2017 - (Recall #: Z-1886-2017)

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 SmartLife Large Aseptic Housing (7126-120-000)

Product Classification:

Class II

Date Initiated: February 28, 2017

Date Posted: May 3, 2017

Recall Number: Z-1886-2017

Event ID: 76739

Reason for Recall:

Stryker Instruments issued a notice of correction for an update to cleaning practices for the Stryker SmartLife Large Aseptic Housings following complaints of deterioration to the housing and the top and bottom housing separating at the weld. Using cleaning practices outside of the HIFU could lead to housing separating at the weld.

Status: Terminated

Product Quantity: 302

Code Information:

Manufacture Start Date for Affected Lots: 18-Mar-2015 Manufacture End Date for Affected Lots: 31-Jan-2017

Distribution Pattern:

Domestic: None Foreign: France, Germany

Voluntary or Mandated:

Voluntary: Firm initiated