DigitalDiagnost Classic recall
DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052
Why was DigitalDiagnost Classic 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: 422102/SN0902020 435210/SN0902204 460471/SN1002019 433651/SN0902114 427610/SN0902108 470160/SN1102003 447013/SN1002008 445778/SN1002006 420208/SN0902019
- Product
- DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052
- 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)