DigitalDiagnost Classic 1.x Upgrades recall
DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081
Why was DigitalDiagnost Classic 1.x Upgrades recalled?
The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
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 Numbers: 456897/SN10000166 402837/SN0802410 2010345 410774/SN0802694
- Product
- DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081
- Recalling firm
- Philips Medical Systems Gmbh, DMC
- Distribution
- US Nationwide; International to 66 countries
- Recall date
- August 29, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)