Neptune 0770100000Recalls & reported problems
Stryker Corporation · SMART DOCKING STATION (120V) · Class 2
All models of Neptune (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- May 6, 2026Class IIOpen, Classified
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable.
Z-2282-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Other APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED devices
- Penumbra System PMX110Penumbra, Inc. · APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED166 reports
- IntelliCart™ 00514010400Zimmer Orthopaedic Surgical Products, Inc. · APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED112 reports
- Penumbra System PMX220Penumbra, Inc. · APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED102 reports
- DeVilbiss 7314P-DDevilbiss Healthcare LLC · Apparatus, Suction, Ward Use, Portable, Ac-Powered69 reports
- PIRANHA 2208011Richard Wolf GmbH · APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED54 reports
- LCSU 4, 800 ml, RTCA Complete Unit 880052Laerdal Medical AS · Apparatus, Suction, Ward Use, Portable, Ac-Powered1 recall0 reports
- Neptune 0711001000Stryker Corporation · APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED1 recall0 reports
- LCSU 4, 300 ml, RTCA Complete Unit 880062Laerdal Medical AS · Apparatus, Suction, Ward Use, Portable, Ac-Powered1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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