← FDA ENFORCEMENT
Z-2354-2026Class II

Philips North America Llc

Recalling firm
Philips North America Llc
Product type
Device
Status
Ongoing
Report date
2026-06-17
Distribution
US distribution to California.
Firm state
MA
Product quantity
1 unit
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & Qualification
Reason for recall

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.

Product description

DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

Code / lot info

Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.

Other recalls SPEQ maps to Validation & Qualification
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See all Validation & Qualification recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.