Philips DigitalDiagnost C90 Recall for Missing Seismic Kit
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Philips North America Llc is recalling one DigitalDiagnost C90 Flex/Value/Chest/ER unit (Model 712035) distributed in California because it was delivered without the required seismic kit.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 28, 2026 and geographically references California. 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
The system was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
Which Products Are Affected
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049. One unit distributed in California. Recall Number: Z-2354-2026.
What You Should Do
Consumers should follow instructions provided in the firm's notification letter.
Why This Matters
The missing seismic kit affects stability of the Wall Stand VS2 during seismic events in the single unit distributed.
Source
FDA recall Z-2354-2026, Philips North America Llc, Cambridge, MA.
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 (732 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 28, 2026.
Frequently Asked Questions
Common questions about this FDA recall.