Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
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Diagnostic Equipment
🏥 Medical Devices • 6,627 recalls
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
ECG Out Cable,for use with a Philips ALS monitor/ defibrillator and bedside monitor for Synchronized cardioversion and Transcutaneous pacing. M1783A/M5526A 12-pin Sync cables, used with HeartStart MRx and HeartStart XL and HeartStart XL+
Philips Electronics North America
Class I - Dangerous
When a Philips monitor/defibrillator is receiving an ECG signal from an auxiliary bedside monitor via a sync cable, the following can occur if the monitor/defibrillator experiences interference from electrical fast transients (EFTs) while connected to AC power: On the HeartStart MRx and HeartStart XL, EFT noise can be misinterpreted as an R-wave. On the HeartStart XL+, EFT noise can disable ECG monitoring, and potentially interrupt demand mode pacing.
Bulk Loader Module for cobas p 512/612 Pre-analytical sample handling that includes de-capping, aliquoting and sorting of samples for analysis. In vitro diagnostic machine component.
Roche Diagnostics Operations
Class I - Dangerous
Possible for sample tubes in the loader to be opened and contaminate the system as well as adjacent samples during processing.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port associated with end-tidal carbon dioxide (EtCO2) monitoring on MRx Monitor/Defibrillators can be pushed into the MRx housing, making it inaccessible. 2. The handle can separate from the MRx housing due to breakage of mounts on the rear case.
Class I - Dangerous
When performing head or neck scans, the currently displayed SAR values could be lower than the actual SAR in the head as predicted by SAR modeling. The predicted HEAD SAR value from the modeling suggests the actual SAR in the head could exceed IEC60601-2-33 limit of 3.2 W/kg for some scans.
Shimadzu C-arm Table, Catalog No. IVS-110, Medical Imaging Table.
Shimadzu Medical Systems
Class I - Dangerous
The C-arm may interfere with the table top under certain circumstances.
Class I - Dangerous
When performing head or neck scans, the currently displayed SAR values could be lower than the actual SAR in the head as predicted by SAR modeling. The predicted HEAD SAR value from the modeling suggests the actual SAR in the head could exceed IEC60601-2-33 limit of 3.2 W/kg for some scans.
CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humans
Innokas Medical Oy
Class I - Dangerous
Monitor may shut down unintentionally without restarting.
Class I - Dangerous
When performing head or neck scans, the currently displayed SAR values could be lower than the actual SAR in the head as predicted by SAR modeling. The predicted HEAD SAR value from the modeling suggests the actual SAR in the head could exceed IEC60601-2-33 limit of 3.2 W/kg for some scans.