Recalls / —
—#141223
Product
Philips Healthcare Xper cardio systems Model : 722123 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and thrombolysis and atherectomics), pacemaker Implantations and electrophysiology (EP). Use of the Allura Xper series system in the OR environment is restricted; the system should only be used for endo-vascular procedures. The Philips Integris Allura 9F is intended for diagnostic cardiovascular, vascular and interventional procedures
- FDA product code
- OWB — Interventional Fluoroscopic X-Ray System
- Device class
- Class 2
- Medical specialty
- Radiology
- 510(k) numbers
- K033737, K041949, K130842, K971365
- Affected lot / code info
- S/N: 3490 3056 3298 3249 3338 3354 3297 3394 3313 3429 3421 3434 3430 3430 3461 3487
Why it was recalled
Monitor Ceiling Suspension system may fall
Root cause (FDA determination)
Process control
Action the firm took
Philips sent an Urgent Field Safety Notice letter dated January 8, 2015 to affected customers. The letter identified the affected product, problem and actions to be taken. The actuator of all affected systems will be replaced free of charge. All affected customers will be contacted in order to schedule the implementation of this action. For questions contact your local Philips representatice: Technical Support Line: 1-800-722-9377.
Recalling firm
- Firm
- Philips Medical Systems, Inc.
- Address
- 3000 Minuteman Rd, Andover, Massachusetts 01810-1032
Distribution
- Distribution pattern
- Worldwide Distribution - US Nationwide and the countries of: Canada,Australia, Austria, Brazil, Chile, China, Denmark, France, Germany, India, Italy, Japan, Mexico, Netherlands, South Africa, Spain, Switzerland and United Kingdom.
Timeline
- Recall initiated
- 2015-02-03
- Terminated
- 2017-01-18
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #141223. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.