Has PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. had other FDA enforcement actions?

Yes. Argus HQ has recorded 199 total FDA actions tied to PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: 0 warning letters, 199 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-01-21; Argus observed and indexed it on 2026-07-16.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Allura Xper FD10; Model Number: 722003;

Name: FDA Recall Record — PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Creator: Argus HQ
Published: 2026-01-21
License: https://argushq.ai/methodology

Event date: 2026-01-21 00:00:00Z
Observed: 2026-07-16 23:20:10Z
Source ID: Z-1064-2026
Payload hash: 47746f5ab1ea9214bfcb44bf…

Summary

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact e… Status: Ongoing.

Entities

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

View source record ↗

Frequently asked questions

Has PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. had other FDA enforcement actions?: Yes. Argus HQ has recorded 199 total FDA actions tied to PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: 0 warning letters, 199 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-01-21; Argus observed and indexed it on 2026-07-16.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

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). PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Allura Xper FD10; Model Number: 722003;. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-philips-medical-systems-nederland-b-v-z-1064-2026

MLA

"PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Allura Xper FD10; Model Number: 722003;." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/events/fda-recall-philips-medical-systems-nederland-b-v-z-1064-2026.

Chicago

Argus HQ Research. "PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Allura Xper FD10; Model Number: 722003;." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-philips-medical-systems-nederland-b-v-z-1064-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_philips_medical_systems_nederland_b_v_z_1064_2026_2026,
  title = {PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Allura Xper FD10; Model Number: 722003;},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-philips-medical-systems-nederland-b-v-z-1064-2026},
  note = {Accessed: July 17, 2026}
}

Informational only. Not legal, financial, or medical advice.