Stryker Instruments Div. of Stryker Corporation: Medical Device Recall in 2015 - (Recall #: Z-2062-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

0210-312-000-Woundcare Replacement kit with soft tip; 0210-318-000; Woundcare Replacement with fan tip; 0210-318-100- Woundcare Replacement Kit; 0210-318-200-Woundcare Replacement with retract coax tip. Accessory to Stryker InterPulse Irrigation System, used for wound debridement, soft tissue debridement, and cleansing of medical, clinical, or surgical sites.

Product Classification:

Class II

Date Initiated: May 8, 2015

Date Posted: July 22, 2015

Recall Number: Z-2062-2015

Event ID: 71271

Reason for Recall:

Potential sterility breach in the packaging.

Status: Terminated

Product Quantity: 5,328 each (444 boxes)

Code Information:

0210-312-000: 12138012, 12203012, 12229012, 12256012, 12293012, 12314012, 12338012, 13086012, 13140012, 13192012; 0210-318-000: 14140012,14258012; 0210-318-100: 12294012,13051012; 0210-318-200: 12143012, 12293012, 13066012, 14037012, 14112012

Distribution Pattern:

Nationwide Distribution-including the states of FL, IA, IL, IN, LA, MD, MN, MO, NC, NM, NY, PA, TN, TX, VA, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated