DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
Reported: August 29, 2018 Initiated: June 27, 2018 #Z-2842-2018
Product Description
DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
Reason for Recall
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.
Details
- Recalling Firm
- Philips Medical Systems Gmbh, DMC
- Units Affected
- 2 units
- Distribution
- US Nationwide; International to 66 countries
- Location
- Hamburg
Frequently Asked Questions
What product was recalled? ▼
DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028. Recalled by Philips Medical Systems Gmbh, DMC. Units affected: 2 units.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 29, 2018. Severity: Moderate. Recall number: Z-2842-2018.
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