Universal Charger Product Usage: The Stryker Universal Battery Charger is designed to be used in conjunction with and pr

FDA device recall Z-1587-2015 · posted 2015-05-07 · Terminated

Recall details

Recalling firm

Stryker Instruments Div. of Stryker Corporation

Reason for recall

The Stryker Universal Battery Charger is not transmitting usage data to the Stryker Cloud as designed. The firm is initiating a software correction to address the issue.

Action taken

Stryker issued e-mail notices to distributors and reps on March 26, 2015 advising that all battery charges would receive a software update to provide a field correction for the upgrade to units to be able to track device usage data to Stryker as designed. There is no customer action required, the chargers will transmit a message to Stryker once the upgrade is complete. Please contact Kelly Jo Davis at 269-389-2921 with any questions.

Root cause

Software design

Status

Terminated

Product code

HWE

Quantity affected

223 chargers

Distribution

US Nationwide in the states of AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, MD, MI, MO, MS, MT, NC, NH, NV, NY, OH, OK, PA, SC, TN, TX, UT, VA, VT, WA, WI and the foreign country of: Canada

Date initiated

2015-03-25

Date posted

2015-05-07

Date terminated

2015-07-08

Location

Portage, MI