PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Allura Xper FD20/15 OR Table; System Code: 722059;
System Code: 722059; UDI: 00884838059122; System Serial Number: 33, 7, 35, 40, 38, 41, 37, 2;
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →