FDA Device Recalls

Recalls /

#64518

Product

Philips Multi Diagnost Eleva

FDA product code
IZISystem, X-Ray, Angiographic
Device class
Class 2
Medical specialty
Radiology
510(k) numbers
K023441
Affected lot / code info
Site numbers 103056, 104136, 521113 102666, 104083, 104530, 105193, 105194, 105394, 504340, 504341, 505039, 505345, 505346, 506155, 506236, 506247, 519574, 532087, 532140, 532151, 532213, 532703, 533312, 533473, 533559, 534247, 535714, 535767, 536019, 536091, 536146, 536720, 536935, 537083, 537669, 537787, 538440, 539457, 539598, 539990, 540252, 541263, 541474

Why it was recalled

Units do not comply with the requirement to provide automatic beam limitation within +/- 3 degrees of horizontal, vertical, and perpendicular to the plane of the image receptor during radiographic procedures.

Root cause (FDA determination)

Other

Action the firm took

On 7/23/07 Philips mailed a letter dated July 9, 2007 titled Electronic Product Radiation Warning. The letter advises customers of the issue and asks that customers apply the enclosed cautionary label to the device. The letter also explains that there will be a system modification to be installed. On 8/20/07 the firm sent the same letter, along with a letter dated 8/20/07 to customers thought to have either scrapped their units and the customer had previously indicated they were no longer using the unit. The 8/20/07 letter requested the customer contact Philps if they are currently using the device.

Recalling firm

Firm
Philips Medical Systems North America Co. Phillips
Address
22100 Bothell Everett Hwy, Bothell, Washington 98021-8431

Distribution

Distribution pattern
Units were distributed to 1543 hospitals and medical centers throughout the US. No international distribution from this firm.

Timeline

Recall initiated
2007-07-23
Posted by FDA
2007-09-25
Terminated
2012-09-17
Status

Source: openFDA Device Recall endpoint. Recall record ID #64518. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.