Stryker Neptune Smart Docking Station Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Stryker Corporation is recalling one Neptune Smart Docking Station due to incomplete manufacturing release and testing, posing a potential electrical shock risk.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 10, 2026 and geographically references Indiana. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
Stryker Corporation initiated a voluntary recall after identifying that one impacted docking station was not released from manufacturing and may not have completed required testing prior to shipment.
Which Products Are Affected
The recall involves the Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System. It is identified by GTIN 07613327634914 and Serial Number 2521008873. One unit was distributed in Indiana.
What You Should Do
Consumers should follow guidance from the recalling firm regarding the affected unit.
Why This Matters
The device may present a potential risk of electrical shock because its safety testing is unverifiable.
Source
FDA recall number Z-2282-2026 (Class II)
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (777 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 10, 2026.
Frequently Asked Questions
Common questions about this FDA recall.