Potential for the outer stainless-steel tube to break or detach.
Diagnostic Equipment
π₯ Medical Devices β’ 6,554 recalls
The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will alarm appropriately.
The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will alarm appropriately.
Potential for the outer stainless-steel tube to break or detach.
Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability.
Potential for the outer stainless-steel tube to break or detach.
Potential for the outer stainless-steel tube to break or detach.
The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will alarm appropriately.
Due to complaints received reporting cracks and/or leaks of the stopcocks associated with the external drainage and monitoring system (EDMS).
The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will alarm appropriately.
Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Hybrid Recon software versions affected are 4.0.0x and 5.0.0
Hermes Medical Solutions AB
Due a potential software/configuration issue that may result is incorrect alignment during reconstructing a SPECT/CT study.
AtellicaΒΏ CH ΒΏ2-Microglobulin (B2M) - In vitro diagnostic use in the quantitative determination of ΒΏ2-microglobulin in human serum and plasma. Siemens Material Number (SMN): 11097635
Siemens Healthcare Diagnostics
Potential for falsely depressed auto-diluted results for samples above the measuring interval of 18.00 mg/L, up to 30.00 mg/L, when using the Atellica CH ΒΏ2-Microglobulin (B2M) reagent.
EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190
Olympus Corporation of the Americas
High-level disinfection ("HLD") with Acecide-C disinfectant in the Olympus OER-Pro Automated Endoscope Reprocessor ("AER") has been removed as a compatible reprocessing method from the Instructions for Use when reprocessing the GIF-1THI90 EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE ( GIF-1TH190 ).
BD identified through potency testing as part of a stability test request to monitor Ampicillin AM-2 due to decrease in potency results of 65% at 18 months, may result in falsely resistant result for ampicillin susceptibility
Mammotrak Diagnostic Coil 1.5T
Philips North America
Potential safety issue where a patient may be harmed while preparing for or during a scan.
SIGNA Architect AIR, Nuclear Magnetic Resonance Imaging System
GE Medical Systems
Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.
Discovery MR750w 3.0T, whole body magnetic resonance scanner
GE Medical Systems
Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.
SIGNA Architect, Nuclear Magnetic Resonance Imaging System
GE Medical Systems
Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.
VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively measures C-reactive protein (CRP) concentration in serum and plasma Model/Catalog Number: 1926740
Ortho-Clinical Diagnostics
May Generate Negatively Biased Results When Testing Samples with High Concentrations of CRP, showing less than upper AMI of 90 mg/L (in the 70-90 mg/L range) while the samples having higher than 90 mg/L. User no way to know if the sample has to be diluted to measure again.
Mammotrak Diagnostic Coil 3.0T
Philips North America
Potential safety issue where a patient may be harmed while preparing for or during a scan.