FDAClass IIOctober 10, 2012

Philips Digital Diagnost with patient carriage recall

Philips Digital Diagnost with patient carriage Model: 712050 with serial number range from 00 000 00 to 09 000 543. Product Usage: Stationary…

Why was Philips Digital Diagnost with patient carriage recalled?

Hook does not securely hold the footplate in vertical position, causing the footplate to disengage and may fall on patient or operator

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial number range (patient carriage) from: 00 000 00 to 09 000 543.

Product
Philips Digital Diagnost with patient carriage Model: 712050 with serial number range from 00 000 00 to 09 000 543. Product Usage: Stationary…
Recalling firm
Philips Healthcare Inc.
Quantity
536 units
Distribution
Worldwide Distribution - US Nationwide and the countries of :Australia, Austria, Bahrain, Belgium, Canada, Chile, China, Czech Republic, Denmark, Finland, , France, Germany, Ireland, Italy, Japan, Netherlands, New Zealand, Norway, Poland, Qatar, Romania, Russia, Saudi Arabia, Sweden, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan. Thailand, Turkey,United Arab Emirates and United Kingdom.
Recall date
October 10, 2012
Classification
Class II
Status
Terminated
Agency
FDA (device)
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