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All product recalls associated with Encision, Inc..
Total Recalls
710
Past Year
38
Class I (Serious)
50
Most Recent
Dec 2025
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.
Firm found pinholes in packaging which would compromise sterility.
iBOT Mobility System may tip over due to malfunction in power base.
Skull pins, which fractured below device specifications during QC testing, were distributed.
Electrosurgical tip may break or come off during use.
Some of the high voltage capacitors in the recalled external defibrillators have had extended charge times resulting in self-test failures following which the defibrillator cannot be used/cannot be turn on.
Some of the high voltage capacitors in the recalled external defibrillators have had extended charge times resulting in self-test failures following which the defibrillator cannot be used/cannot be turn on.
Some of the recalled defibrillator batteries contain an incorrect fuse which could open resulting in a defibrillator which will not work.
Some of the recalled defibrillator batteries contain an incorrect fuse which could open resulting in a defibrillator which will not work.
The recall includes certain 20-, 21-, and 22-inch walk-behind lawn mowers; certain 30-inch mid-engine riding lawn mowers; certain 38-, 40-, 42-, and 46-inch lawn tractors; and certain 46-inch garden tractors. They are red, black or gray. "Murray" is written on the body of the mowers. The model number can be found on the unit's nameplate located under the seat of the lawn tractors and at the rear of the mower housing on the walk-behind mowers. The following model numbers are included in recall: 309029X92 387002X92 405000X8 425620X92 425001X8 425014X92 425015X92 461004X92 465306X8 201010X18 20112X92 218950X92 22265X8 223310X8 224110X8 225113X92 226111X92
These 40- and 42-inch-cut lawn tractors come with a 1.4 gallon remote fuel tank. They come in red and black or all black. The model number can be found on a nameplate located under the seat. The following model numbers are included in recall: 40507X8 40536X4 405618X81 42504X71 42504X99 42510 42512X99 42542X6 42543X6 425610X99 425612X99 42575X81
Potential for saved blood flow velocity values to not agree with actual velocity values as shown on the spectrogram axis.
The device is not stable throughout its labeled expiration date.
Seal integrity, sterility not assured.
Lot is being recalled because some of the kits contain an incorrect guidewire.
The kits were packaged with incorrect dispensing pipettes.
Incorrect calibration standard value may result in 25% higher assay values for controls and patient samples
Product's outer carton label was labeled with an extended expiration date
The kits are producing lower values than expected, which may result in an increase of false positive test results.
Use of NC versions of AEM monitor presents burn hazard when used with single pad and capacitively coupled patient return electrodes.
Use of NC versions of AEM monitor presents burn hazard when used with single pad and capacitively coupled patient return electrodes.