Philips recalls foot switches for Allura Xper FD systems that may bend on non-flat surfaces, causing fluoroscopy image issues. Affected units include specific model numbers and systems.
Additional units have been identified for previous recall Z-1280-2016 (RES 69339): If a Footswitch is frequently used on a non-flat surface or in the pedestal, the footswitch pedals may get bent. This might cause an intermittent or continuous inability of making live fluoroscopy images or exposures.
Philips is recalling foot switches used with Allura Xper FD series medical imaging systems. If these switches bend from being used on uneven surfaces, they can cause intermittent or continuous failures in fluoroscopy imaging.
Frequently using the foot switches on non-flat surfaces or within the pedestal can cause the pedals to bend. This bending may lead to intermittent or continuous inability to produce live fluoroscopy images or exposures during medical procedures.
Medical professionals using Philips Allura Xper FD series imaging systems with the recalled foot switches are most at risk. Patients undergoing fluoroscopy procedures may be affected if the imaging fails.
Check if your foot switch model number is 452270000141, 452270000151, 452270000142, 452270000381, 452270000382, 459800076001, 459800076021, 459800415571, 459800415581, 459800415531, or 459800415561. These switches are used with specific Allura Xper FD series systems listed in the recall.
Identify your foot switch model number to confirm if it is one of the recalled models listed in the recall notice.
Use the foot switch on flat surfaces and avoid placing it within the pedestal to prevent bending.
The recalled foot switches are used with Philips Allura Xper FD series systems, including specific model numbers like 722001 Allura Xper FD 10 C and others listed in the recall notice.
If the foot switch bends from being used on non-flat surfaces or within the pedestal, it may cause intermittent or continuous inability to make live fluoroscopy images or exposures.
No, but you should ensure the foot switch is used on flat surfaces and not within the pedestal to prevent bending. The recall does not require immediate discontinuation.
We’ve drafted a message you can send Philips Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1141-2019 — Philips Medical Systems Philips Medical Systems Hello, I own a Philips Medical Systems that is covered by recall Z-1141-2019 from Philips Medical Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
