Recall Z-0903-2014— Stryker Instruments Div. of Stryker Corporation

Name: FDA recall Z-0903-2014
Creator: U.S. Food and Drug Administration
Published: 2013-12-30

Class II · Terminated

Class II FDA medical device recall by Stryker Instruments Div. of Stryker Corporation, initiated 2013-12-30, terminated 2016-01-12. It names one FDA 510(k) clearance: K132671. Product: Neptune 2 Rover Ultra Waste Management System. Reason: The purpose of this correction is to upgrade the Neptune 2 Waste Management Systems in the field to the recently obtained 510(k) clearance specifications..

Recalling firm: Stryker Instruments Div. of Stryker Corporation
Classification: Class II
Status: Terminated
Initiated: 2013-12-30
Terminated: 2016-01-12
Firm location: Portage, MI, United States

510(k) clearances named in this recall

1 on FDA's record

K132671 — STRYKER NEPTUNE 2 WASTE MANAGMENT SYSTEMStryker Corporation·cleared 2013-12-20

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Neptune 2 Rover Ultra Waste Management System

Reason for recall

The purpose of this correction is to upgrade the Neptune 2 Waste Management Systems in the field to the recently obtained 510(k) clearance specifications.

Data sourced from openFDA. This site is unofficial and independent of the FDA.