Loading...
Loading...
All product recalls associated with ela Medical Llc.
Total Recalls
1000
Past Year
1000
Class I (Serious)
127
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Analysis showed that the screwdriver was not fully inserted in the setscrew's hex cavity, which damaged the setscrew.
The product is being recalled because the patient support may travel downwards without being commanded to move.
Only Gotham Compact Fluorescent Downlights sold with the optional backup battery pack are included in the recall. The lights are recessed ceiling lights that were manufactured between November 1, 2007 and July 31, 2008.
Images not correlated: A leak between the Tube Interface and the Outlet Tube of the transducer may result in a failure to produce respiratory correlated images.
Incorrect result: The absorbance has changed as the standards have aged; the standards' turbidity has become denser. The recalled lot is now reading 0.15 ABS @ 625 nm. TREK'S internal specification and the manufacturer's (Hardy Diagnostics) specification is 0.08 - 0.10 ABS @625 nm. CLSI specifies 0.08 - 0.13 ABS @ 625 nm.
Leaks: Infusion Cuffs may exhibit air leakage at the union of the tube and bag, and not maintain pressure. For further information, please contact the firm at 203-488-6056.
Leaks: Infusion Cuffs may exhibit air leakage at the union of the tube and bag, and not maintain pressure. For further information, please contact the firm at 203-488-6056.
Leaks: Infusion Cuffs may exhibit air leakage at the union of the tube and bag, and not maintain pressure. For further information, please contact the firm at 203-488-6056.
Leaks: Infusion Cuffs may exhibit air leakage at the union of the tube and bag, and not maintain pressure. For further information, please contact the firm at 203-488-6056.
Water may collect and freeze in the vent pipe. This can rupture the magnet vessel during a cryogen transfer, and release helium into the MRI suite.
Water may collect and freeze in the vent pipe. This can rupture the magnet vessel during a cryogen transfer, and release helium into the MRI suite.
Water may collect and freeze in the vent pipe. This can rupture the magnet vessel during a cryogen transfer, and release helium into the MRI suite.
Water may collect and freeze in the vent pipe. This can rupture the magnet vessel during a cryogen transfer, and release helium into the MRI suite.
Water may collect and freeze in the vent pipe. This can rupture the magnet vessel during a cryogen transfer, and release helium into the MRI suite.
Water may collect and freeze in the vent pipe. This can rupture the magnet vessel during a cryogen transfer, and release helium into the MRI suite.
Some units may contain the wrong filter, which does not have the proper lock and may result in a leak.
Product was assembled incorrectly and connected to the wrong part.
Standardization of the reagent performance data did not match the standardization used to assign the calibrator values.
This recall involves Apeks TX, ATX, and XTX second stage regulators that have never been serviced. Apeks and TX, ATX, or XTX is printed on the regulator.
The recalled utility vehicle is Model 620i. The model number is painted on the side of the vehicle. The recall includes the following serial numbers. The serial number plate is on the vehicle's frame in front of the passenger side rear fender. Model Serial Number Ranges XUV 620i Gas (Como) M0XUVGC020001 thru M0XUVGC020959 XUV 620i Gas (Olive) M0XUVGT021581 thru M0XUVGT021808 XUV 620i Gas (Green) M0XUVGX023930, M0XUVGX023941, M0XUVGX023956, M0XUVGX023961 thru M0XUVGX023962 M0XUVGX023968 thru M0XUVGX025507