Z-0903-2014 Class II Terminated
FDA device recall Z-0903-2014 was initiated by Stryker Instruments Div. Of Stryker Corporation on Dec 30, 2013 and is designated Class II. 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. The recall status is terminated (terminated Jan 12, 2016).
Recall details
- Product Type
- Devices
- Report Date
- Feb 12, 2014
- Initiation Date
- Dec 30, 2013
- Termination Date
- Jan 12, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
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.
Distribution pattern
Nationwide and Canada, Germany, Australia, New Zealand
Code information
Manufacturer Part Number 0702-002-000 (230V) All serial numbers
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0903-2014
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026