1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices)
Reported: February 2, 2022 Initiated: January 21, 2022 #Z-0526-2022
Product Description
1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices)
Reason for Recall
Friction rubber block in the clamping mechanism was missing in the Footrest. It may slip down along the patient table while in use with a patient. This accessory is designed to use with Intelli-C, Right and Intelli-C, Left.
Details
- Recalling Firm
- NRT X-RAY A/S
- Units Affected
- 72 units
- Distribution
- USA: IA, KY,LA, MA, NC,NY, OH, SC, WA, WV OUS: Switzerland, Czech Republic, Germany, Denmark, Netherlands, RSA, Sweden
- Location
- Hasselager
Frequently Asked Questions
What product was recalled? ▼
1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C devices). Recalled by NRT X-RAY A/S. Units affected: 72 units.
Why was this product recalled? ▼
Friction rubber block in the clamping mechanism was missing in the Footrest. It may slip down along the patient table while in use with a patient. This accessory is designed to use with Intelli-C, Right and Intelli-C, Left.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 2, 2022. Severity: Moderate. Recall number: Z-0526-2022.
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