Carestream Health, Inc. recalls DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagnostic quality radiographic images to…
After pressing and releasing the Z-Axis Motorized buttons on the Tube Head Display, the Overhead Tube Crane (OTC) could potentially continue the movement unexpectedly to a certain distance which could potentially…
Read the official notice →- Date
- 2023-03-08
- Country
- United States
- Brand
- Carestream Health
- Product
- DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagnostic quality radiographic images to aid…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide distribution in the states of…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Carestream Health recalls
- 2023-12-13
USCarestream Health, Inc. recalls DRX Revolution Mobile X-Ray System
Unexpected failure of electrical components within the CPI generator.
FDA · DeviceCarestream Health, Inc.Worldwide Distribution: US (Nationwide Distribution); and OUS (Foreign):…Official notice →- 2023-11-15
- US
Carestream Health, Inc. recalls The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray system utilizing digital radiography (DR) technology. the system…
There is a potential for unexpected failure of the electrical components within the Carestream Health Inc. generator installed in your DRX-Revolution Mobile X-ray System(s). This can lead to temporary and self…
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- US
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Biomerieux Inc recalls MYLA comprises AST Filters in conjunction with VITEK MS; middleware which connects microbiology laboratory instruments for ID/AST and…
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FDA · DeviceBiomerieux IncUS Nationwide distribution to the states of Alabama, California, North…Official notice →