CombiDiagnost R90 R.1.0
Reported: May 24, 2023 Initiated: March 3, 2023 #Z-1588-2023
Product Description
CombiDiagnost R90 R.1.0
Reason for Recall
Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0, CombiDiagnost R90 R.1.0 and CombiDiagnost R90 R1.1 systems are missing a certification label required by the Food and Drug Administration (FDA).
Details
- Recalling Firm
- Philips North America
- Units Affected
- 25 systems in total
- Distribution
- US Nationwide
- Location
- Cambridge, MA
Frequently Asked Questions
What product was recalled? ▼
CombiDiagnost R90 R.1.0. Recalled by Philips North America. Units affected: 25 systems in total.
Why was this product recalled? ▼
Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0, CombiDiagnost R90 R.1.0 and CombiDiagnost R90 R1.1 systems are missing a certification label required by the Food and Drug Administration (FDA).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 24, 2023. Severity: Moderate. Recall number: Z-1588-2023.
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