Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost Recalled by Philips Medical Systems, Inc. Due to The hook does not securely hold the footplate...
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
Patient Support Material Number: 9890 010 87431 used with: BuckyDiagnost ; Model: 704060/706037
Quantity: 1517 systems, not all units have the patient support accessory
Why Was This Recalled?
The hook does not securely hold the footplate in vertical position. Therefore the footplate can fall or swing down and may hurt the operator or patient.
Where Was This Sold?
This product was distributed to 11 states: AZ, CT, FL, HI, KY, MA, MN, NC, TX, VA, WY
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