Reported Sep 6, 2023 · Ongoing
Wireless Foot Switch distributed with Philips Allura Xper and Azurion Interventional Fluoroscopic X-Ray Systems
Philips Medical Systems Nederland B.v.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 4-6 · Best, N/A · N/A
Is this the product you have?
- Wireless Foot Switch distributed with Philips Allura Xper and Azurion Interventional Fluoroscopic X-Ray Systems
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Barcodes Product as published 722001722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722015, 722023, 722025, 722026, 722027, 722028, 722029, 722033, 722035, 722038, 722039, 722058, 722059, 722064, 722065, 722066, 722067, 722068, 722078, 722079 — No UDI-DI — 459800772231459800772233459800772261459800772263459800415531459800415532459800415533459800415534459800415535459800415571459800415572459800415573459800415574459800415575Lot No. 459800772231, 459800772233, 459800772261, 459800772263, 459800415531,459800415532, 459800415533, 459800415534, 459800415535, 459800415571, 459800415572, 459800415573, 459800415574, 459800415575. - Amount recalled
- 1865 units
Where it was sold
- Nationwide
Why it was recalled
Loss of availability of the wireless foot switch during procedures.
This product could cause temporary or reversible health problems — stop using it.
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