Urodiagnost recall
Urodiagnost, Product No. 708033 Product Usage: The Philips UroDiagnost MRF can be used to perform all urological and gynecological routine…
Why was Urodiagnost recalled?
The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.
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 codes 1 2 3 4 5 7 8 11 13 14 15 16 17 18 21 48 59 60 64
- Product
- Urodiagnost, Product No. 708033 Product Usage: The Philips UroDiagnost MRF can be used to perform all urological and gynecological routine…
- Recalling firm
- Philips North America, LLC
- Quantity
- 1969
- Distribution
- US Nationwide domestic distribution, and worldwide international distribution.
- Recall date
- April 3, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)