Use cautionMedical device recall · FDA · Published December 3, 2024
Stryker Neptune Rover Recalls: Loose Bolts May Cause Suction Failure
Stryker recalls Neptune 3 Rover and S Rover models with loose bolts that could cause suction failure during procedures. Affected units have specific model numbers and lot numbers.
Bolts on the vacuum pump filter housing and the flange plate were not properly tightened, impacting the function of the Neptune rovers. Systems with loose bolts may fail to provide sufficient suction force or loss of suction during a procedure.
Take action
Contact the company
📍Recalling firmStryker Corporation1941 Stryker Way · Portage, MI 49002-9711
“Stryker Neptune Rover Recalls: Loose Bolts May Cause Suction Failure.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53367-stryker-neptune-rover-recalls-loose-bolts-may-cause-suction-failure. Based on FDA recall #Z-0807-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0807-2025%22&limit=1).
The FDA announced on Dec. 3, 2024, that Stryker Corporation is recalling Neptune rovers due to loose bolts that may cause suction failure during procedures. The agency issued the recall under number Z-0807-2025.
How to tell if you have it
100V NEPTUNE 3 ROVER JAPANESE (0703-003-000)
120V NEPTUNE S ROVER (0711-001-000)
230V NEPTUNE 3 ROVER ENGLISH (0703-002-000ENG)
230V NEPTUNE 3 ROVER SPANISH (0703-002-000ES)
GTIN 07613327382082, Lot Numbers: 2427418723, 2427423863, 2427418453, 2427423873, 2427418743, 2427419773
GTIN 07613327382068, Lot Numbers: 2427418453
GTIN 07613327381948, Lot Numbers: 2427418093, 2427418053, 2427418073, 2427418233, 2427418013, 2427418723
Bolts on the vacuum pump filter housing and the flange plate were not properly tightened, impacting the function of the Neptune rovers. Systems with loose bolts may fail to provide sufficient suction force or loss of suction during a procedure.
Context
GovInfoNow's records show Stryker Corporation has 34 other recalls on record since 2017-11-17. Other recent recalls include the Stryker Ahto Dual Spike Tube Set (2026-06-08), the Stryker Neptune Smart Docking Station (2026-05-06), and the Stryker FluidSmart Urology Tube Set (2026-04-09). Additional recent recalls of similar products include the Stryker Hoffmann II Connecting Rod Micro 3 x 50mm (2026-07-01), the Stryker Hoffmann II Connecting Rod Micro 3 x 120mm (2026-07-01), and the Genesis Push-In Suture Anchor (2025-12-17).
How to tell if you have this one
Check for model numbers: 100V NEPTUNE 3 ROVER JAPANESE (0703-003-000), 120V NEPTUNE S ROVER (0711-001-000), or 230V NEPTUNE 3 ROVER ENGLISH/SPANISH. Lot numbers include specific sequences like 2427418723 or 2429720623.
Brand
Stryker
Product
100V NEPTUNE 3 ROVER JAPANESE (0703-003-000) 120V NEPTUNE S ROVER (0711-001-000) 230V NEPTUNE 3 ROVER ENGLISH
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Model and Lot Numbers
Identify the model number and lot numbers from the product labels or documentation to confirm if the device is affected.
Contact Stryker for Details
Reach out to Stryker Corporation directly for specific instructions on whether your device is affected and what actions to take.
Where it went and when
Where it was distributed
Distributed in 3 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “US (Domestic) distribution to states of: WA, GA, and IL. OUS (International) distribution to Japan and Netherlands.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Georgia, Illinois, Washington.
Recall timeline
FDA published this recall 43 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0807-2025 (December 3, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0807-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.