CLASS II Device recall · Reported 12 Feb 2014 · FDA Enforcement Report

Neptune 2 Rover Ultra Waste Management System recalled

Stryker Instruments Div. of Stryker is recalling Neptune 2 Rover Ultra Waste Management System, distributed nationwide in the US. The recall was initiated on 30 Dec 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesManufacturer Part Number 0702-001-000 (120V) All serial numbers

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0902-2014
FDA event ID: 67191
Recalling firm: Stryker Instruments Div. of Stryker, Portage, MI
Classification: Class II
Status: Terminated
Recall initiated: 30 Dec 2013
FDA classified: 31 Jan 2014
Reported: 12 Feb 2014
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

30 Dec 2013	Recall initiated by company
31 Jan 2014	Classified by FDA	+32 days
12 Feb 2014	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Product as listed by the FDA

Neptune 2 Rover Ultra Waste Management System.

Where it was distributed

Nationwide and Canada, Germany, Australia, New Zealand

Nationwide

Questions about this recall

Why was it recalled?

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.

Which lots are affected?

Manufacturer Part Number 0702-001-000 (120V) All serial numbers

Where was it sold?

Nationwide and Canada, Germany, Australia, New Zealand

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 67191

Reported	Class	Recall	Company	Reason	Where
12 Feb 2014	CLASS II	Neptune 2 Rover Ultra Waste Management System recalled	Stryker Instruments Div. of Stryker	Other	Nationwide

More recalls from Stryker Instruments Div. of Stryker

All 161

Reported	Class	Recall	Company	Reason	Where
27 Jul 2022Device	CLASS III	Triton Sponge System recalled by Stryker Instruments Div. of	Stryker Instruments Div. of Stryker	Device Malfunction	Nationwide
27 Jul 2022Device	CLASS II	Triton Canister System (finished part numbers FG recalled	Stryker Instruments Div. of Stryker	Device Malfunction	Nationwide
27 Jul 2022Device	CLASS II	SurgiCount+ System Application recalled by Stryker Instruments Div. of	Stryker Instruments Div. of Stryker	Device Malfunction	KS, ME
18 Nov 2020Device	CLASS II	Stryker Zyphr Disposable Cranial Perforator recalled	Stryker Instruments Div. of Stryker	Foreign Material	Nationwide
6 May 2020Device	CLASS II	Neptune E-sep Blade Electrode recalled by Stryker Instruments Div. of	Stryker Instruments Div. of Stryker	Other	MI

Other Other Medical Devices recalls

All 13,778

Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Device	CLASS II	Citric Complete Dry Citric Acid Concentrate recalled	Nipro Renal Soultions USA	Other	Nationwide
16 Sep 2026Device	CLASS I	Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS II	Halyard IV Start Kit Non-Sterile recalled by Avid Medical	Avid Medical	Sterility	Nationwide
16 Sep 2026Device	CLASS I	Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries	Medical Action Industries Inc. 306	Sterility	6 states
16 Sep 2026Device	CLASS II	AMS Convenience Kit: Dsaek Pack - RX recalled	Windstone Medical Packaging	Device Malfunction	Nationwide