PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has been the subject of 199 FDA enforcement/approval records tracked by Argus HQ, compared to 3 for Stryker Leibinger GmbH & Co. KG.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: 0 warning letters, 199 recalls, 0 approval records, 0 Form 483s.
Stryker Leibinger GmbH & Co. KG: 0 warning letters, 3 recalls, 0 approval records, 0 Form 483s.
Side by side
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Warning letters0
Stryker Leibinger GmbH & Co. KG — Warning letters0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Recalls199
Stryker Leibinger GmbH & Co. KG — Recalls3
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Approval records0
Stryker Leibinger GmbH & Co. KG — Approval records0
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Form 483s0
Stryker Leibinger GmbH & Co. KG — Form 483s0
Timeline
Cite this comparison
Pre-formatted for a story, footnote, or reference list:
"PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. vs Stryker Leibinger GmbH & Co. KG: FDA Enforcement Comparison." Argus HQ, accessed July 17, 2026. https://argushq.ai/compare/philips-medical-systems-nederland-b-v-vs-stryker-leibinger-gmbh-and-co-kg
Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗

