Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some identified Ingenia systems shipped between December...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Medical Systems, Inc. directly.
Affected Products
Ingenia 3.0T, magnetic resonance imaging system.
Quantity: 18
Why Was This Recalled?
For some identified Ingenia systems shipped between December 2013 and March 2014, cover set rear magnetic M10 nuts were erroneously supplied instead of A4 stainless steel nuts.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems, Inc.
Philips Medical Systems, Inc. has 65 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report