Z-2062-2012 Class I Terminated

Recalled by Stryker Instruments Div. Of Stryker Corporation — Portage, MI

FDA device recall Z-2062-2012 was initiated by Stryker Instruments Div. Of Stryker Corporation on Jun 8, 2012 and is designated Class I. Reason for recall: Stryker has received two reports of serious injury as a result of tissue damage associated with the use of the Neptune 2, including an event in which one customer connected the Neptune 2 System to a… The recall status is terminated (terminated Aug 23, 2016). Affected quantity: 5925 domestic 2 international.

Recall details

Product Type
Devices
Report Date
Aug 22, 2012
Initiation Date
Jun 8, 2012
Termination Date
Aug 23, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
5925 domestic 2 international

Product description

Neptune 1 Gold Rover (120 Vand 230V ) Waste Management System Part Number 0700-001-000, 0700-002-000(International) Instructions For Use 0700-001-700, 0700-002-707 Intended for use in the surgical environment or physician's office to collect and dispose of surgical fluid waste.

Reason for recall

Stryker has received two reports of serious injury as a result of tissue damage associated with the use of the Neptune 2, including an event in which one customer connected the Neptune 2 System to a passive chest drainage tube post operatively, resulting in a fatality. The current IFU did not specifically warn against connecting all Neptune Waste Management devices, which is a high vacuum/high flow device, to a passive drainage tube. June 12, 2012, customers were instructed to review the revised IFU, distribute to affected departments, and educate users of the Neptune on this warning. Warning Labels, which are pending distribution, are required on all Neptune devices. Further investigation found the Neptune 1 Silver, Neptune 2 Ultra (120V) and Neptune 2 Ultra (230V) lacked FDA 510(k) clearance and therefore are not legally marketed without determination of their safety and effectiveness. FDA advises Neptune 1 Silver, Neptune 2 Ultra (120V) and Neptune 2 Ultra (230V) not be used. However, customers who do not have an alternative device to use should weigh the risks and benefits associated with continued use of these devices. If customers choose to continue use of the Neptune Silver, Neptune 2 Ultra (120V) or Neptune 2 (230V), they must complete a Certificate of Medical Necessity and return it to Stryker by October 12, 2012.

Distribution pattern

Worldwide Distribution -- USA (nationwide) and country of: Canada. .

Code information

120V Gold part numbers 0700-001-000 IFU 0700-001-700 230 V Gold 0700-002- 000, IFU 0700-002-707 Neptune 1 Gold Rover 0700-001-000 1/11/01  12/23/09 3/26/01  1/30/10 0700-001-700 Neptune 1 Gold Rover - International 0700-002-000 9/15/05 10/3/05  10/3/05 0700-002-707

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-2062-2012
openFDA file date
Nov 10, 2026
Loaded by RegDataLab
Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for Z-2062-2012. Report a data issue: hello@regdatalab.com.