NRT X-RAY A/S recalls 1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C…
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,…
Read the official notice →- Date
- 2022-02-02
- Country
- United States
- Brand
- Nrt X-Ray A/S
- Product
- 1. Footrest ( use exclusively in combination with Intelli-C devices) 2. Shoulder support ( use exclusively in combination with Intelli-C…
- Classification
- Class II
- Units
- USA: IA, KY,LA, MA, NC,NY, OH, SC, WA, WV OUS: Switzerland, Czech Republic,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Nrt X-Ray A/S recalls
- 2024-05-15
USNRT X-RAY A/S recalls Intelli-C: Right side suspended Tabletop, REF: 03400000; Left side suspended Tabletop, REF: 03400010, used with the Intelli-C X-ray system
X-ray system C-arm may experience uncontrolled motion if 1) AC motor controller firmware has a faulty setting, 2) the Motor/gear assembly is worn, 3) CAT movement is driven at maximum speed and angulated more than 75…
FDA · DeviceNRT X-RAY A/SUS Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, WV,…Official notice →- 2023-06-07
- US
NRT X-RAY A/S recalls Intelli-C, Left side suspended Tabletop, REF: 03400010
There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes the detector to move until it is stopped by the movement end-stop.
FDA · DeviceNRT X-RAY A/SUS Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA,…Official notice →
Other drugs & medical recalls in the United States
- 2022-02-02
- US
FlexDex Inc. recalls 8mm FlexDex Needle Driver, Product Code FD-335 ND
The firm is reinforcing the IFU instructions: "Do not use if the package is damaged." If upon inspection of the packaging, any damage is observed, including pinholes or tears in the pouch, the product should not be used.
- US
NuVasive Specialized Orthopedics, Inc. recalls MAGEC 1 System
Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015.
- US
Velano Vascular recalls PIVO Blood Collection Device 20G, REF: 202-0005
Incomplete sealing of blood collection device unit packages may produce a breach in the sterile barrier enclosing the product. This could lead to microbial contamination of the device prior to use. The health effects…
FDA · DeviceVelano VascularUS Nationwide distribution in the states of CT, CO, UT, PA, IL, WA, CA, NJ,…Official notice → - US
Biomerieux Inc recalls API ID 32 C Strips, Reference 32200, Rx Only, IVD API ID 32 C is a qualitative standardized system for the identification of yeasts. It…
Risk of misidentification or delayed results with the absence of identification due to thermoforming defect.
FDA · DeviceBiomerieux IncUS (Domestic) Distribution to states of: AZ, IA, KY, and NY.Official notice → - US
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Sector DICOM"
The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
FDA · DeviceGE Healthcare, LLCDomestic: AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY,…Official notice → - US
Siemens Medical Solutions USA, Inc recalls Artis pheno with software VE20C- diagnostic imaging angiography system Model: 10849000
Four potential software issues with Artis pheno and Artis icono systems with software VE20C: 1. Updated calibration data not saved with measurement after scene+/-; 2. No x-ray possible, system shutdown/restart might be…