Stryker Neptune 3 and S Rovers Recalled for Potential Suction Loss

Agency Publication Date: January 6, 2025

Summary

Stryker Corporation is recalling 14 units (expanded to 21 units) of the Neptune 3 and Neptune S Rovers, which are surgical suction systems used in medical procedures. This recall was initiated because bolts on the vacuum pump filter housing and the flange plate were not properly tightened during manufacturing. This defect can lead to insufficient suction or a total loss of suction force during a procedure, though no injuries have been reported to date.

Risk

The loose bolts can cause the suction system to malfunction or fail entirely while it is being used during surgery. This loss of suction could delay medical procedures or prevent the necessary removal of fluids from a patient's body, posing a risk to patient safety.

What You Should Do

This recall affects Stryker Neptune 3 and Neptune S Rovers, specifically the 100V Japanese, 120V S Rover, and 230V English and Spanish models.
Identify your device by checking the model number and lot number on the device label. Affected models include 0703-003-000, 0711-001-000, 0703-002-000ENG, and 0703-002-000ES. See the Affected Products section below for the full list of affected codes.
Stop using the recalled device immediately to prevent sudden loss of suction during a medical procedure.
Contact Stryker Corporation or your local distributor to arrange for a return, replacement, or correction of the device.
For additional questions, call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

Other Action

How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: 100V NEPTUNE 3 ROVER JAPANESE

Variants: 100V, Japanese

Model / REF:

0703-003-000

Lot Numbers:

2427418093

2427418053

2427418073

2427418233

2427418013

2427418723

GTIN:

07613327381948

Firm initiated voluntary recall.

Product: 120V NEPTUNE S ROVER

Variants: 120V

Model / REF:

0711-001-000

Lot Numbers:

2429720623

2429721033

2429720903

2429721203

2429720973

2429721223

2429721023

2303501403

2323610223

2403600253

GTIN:

07613327576887

Firm initiated voluntary recall.

Product: 230V NEPTUNE 3 ROVER ENGLISH

Variants: 230V, English

Model / REF:

0703-002-000ENG

Lot Numbers:

2427418723

2427423863

2427418453

2427423873

2427418743

2427419773

GTIN:

07613327382082

Firm initiated voluntary recall.

Product: 230V NEPTUNE 3 ROVER SPANISH

Variants: 230V, Spanish

Model / REF:

0703-002-000ES

Lot Numbers:

2427418453

GTIN:

07613327382068

Firm initiated voluntary recall.

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 95856

Status: Active

Manufacturer: Stryker Corporation

Sold By: Stryker Corporation

Manufactured In: United States

Units Affected: 14 (Expanded to 21 units on 10/9/25)

Distributed To: Washington, Georgia, Illinois

Agency Last Updated: November 19, 2025

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.

Summary

What You Should Do

This recall affects Stryker Neptune 3 and Neptune S Rovers, specifically the 100V Japanese, 120V S Rover, and 230V English and Spanish models.

Identify your device by checking the model number and lot number on the device label. Affected models include 0703-003-000, 0711-001-000, 0703-002-000ENG, and 0703-002-000ES. See the Affected Products section below for the full list of affected codes.

Stop using the recalled device immediately to prevent sudden loss of suction during a medical procedure.

Contact Stryker Corporation or your local distributor to arrange for a return, replacement, or correction of the device.

For additional questions, call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Affected Products

Product: 100V NEPTUNE 3 ROVER JAPANESE

Variants: 100V, Japanese

Model / REF:

0703-003-000

Lot Numbers:

2427418093

2427418053

2427418073

2427418233

2427418013

2427418723

GTIN:

07613327381948

Firm initiated voluntary recall.

Product: 120V NEPTUNE S ROVER

Variants: 120V

Model / REF:

0711-001-000

Lot Numbers:

2429720623

2429721033

2429720903

2429721203

2429720973

2429721223

2429721023

2303501403

2323610223

2403600253

GTIN:

07613327576887

Firm initiated voluntary recall.

Product: 230V NEPTUNE 3 ROVER ENGLISH

Variants: 230V, English

Model / REF:

0703-002-000ENG

Lot Numbers:

2427418723

2427423863

2427418453

2427423873

2427418743

2427419773

GTIN:

07613327382082

Firm initiated voluntary recall.

Product: 230V NEPTUNE 3 ROVER SPANISH

Variants: 230V, Spanish

Model / REF:

0703-002-000ES

Lot Numbers:

2427418453

GTIN:

07613327382068

Firm initiated voluntary recall.