What should someone who has this product do?

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.) and recall number Z-2354-2026, then follow Philips North America Llc's recall instructions.

Has Philips North America Llc had other FDA recalls or enforcement actions?

Yes. Argus HQ has recorded 4 total FDA actions tied to Philips North America Llc, including 4 recalls and 0 warning letters.

FDA Recall Database: Class II Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. by Philips North America Llc

Philips North America Llc recalled DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. on 2026-06-17. FDA classified this action as a Class II recall (recall number Z-2354-2026). 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.. Recall status: Ongoing. This is a device-category FDA recall record.

Key facts

Recalling firm	Philips North America Llc
Manufacturer	Not disclosed in the FDA record.
Brand name	Not disclosed in the FDA record.
Product description	DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Classification	Class II
Recall number	Z-2354-2026
Report date	Not disclosed in the FDA record.
Status	Ongoing
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.

What this classification means

FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is Philips North America Llc and the affected product is described in FDA's record as: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.. FDA's stated reason for the recall is: 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.. The recall is tracked under FDA recall number Z-2354-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do. Recall status can change while FDA and the recalling firm continue corrective actions, so checking the firm's own notice for the most current guidance is recommended. Adverse events believed to be related to a recalled product can be reported to FDA's MedWatch program, which FDA uses to monitor safety signals after a recall is opened.

What consumers should do

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. -- and the recall number Z-2354-2026. If it matches, stop using or distributing it and contact Philips North America Llc or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do.

Philips North America Llc’s FDA history

Argus HQ has recorded 4 total FDA actions tied to Philips North America Llc: 0 warning letters, 4 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

What was recalled and why?: Philips North America Llc recalled DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.. FDA's record states the reason for recall as: 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.. The recall is logged under FDA recall number Z-2354-2026 with a Class II classification.
How serious is this recall?: FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote.
What should someone who has this product do?: Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.) and recall number Z-2354-2026, then follow Philips North America Llc's recall instructions.
Has Philips North America Llc had other FDA recalls or enforcement actions?: Yes. Argus HQ has recorded 4 total FDA actions tied to Philips North America Llc, including 4 recalls and 0 warning letters.

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Full FDA history for Philips North America Llc

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). FDA Recall Database: Class II Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. by Philips North America Llc. Digital Empire LLC. Retrieved from https://argushq.ai/recall/fda-recall-philips-north-america-llc-z-2354-2026

MLA

"FDA Recall Database: Class II Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. by Philips North America Llc." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/recall/fda-recall-philips-north-america-llc-z-2354-2026.

Chicago

Argus HQ Research. "FDA Recall Database: Class II Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. by Philips North America Llc." Digital Empire LLC. Accessed July 13, 2026. https://argushq.ai/recall/fda-recall-philips-north-america-llc-z-2354-2026.

BibTeX

@misc{argushq_argushq_ai_recall_fda_recall_philips_north_america_llc_z_2354_2026_2026,
  title = {FDA Recall Database: Class II Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. by Philips North America Llc},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/recall/fda-recall-philips-north-america-llc-z-2354-2026},
  note = {Accessed: July 13, 2026}
}

Source: FDA.gov — Recalls ↗