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All product recalls associated with Heather's Choice.
Total Recalls
1000
Past Year
592
Class I (Serious)
65
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.
Heather's Choice Salmon Chowder is being recalled because the firm operated without a permit and lack a HACCP plan. This product also contains undeclared coconut.
Heather's Choice Rancheros is being recalled because the firm operated without a permit and lack a HACCP plan.
This recall involves Craftsman 3-in-1 high-wheel, gas-powered, push mowers equipped with Honda GCV160 engines and a 21-inch deck. The mowers have a black engine control/bail lever, engine shroud and deck with 12-inch rear wheels and a gray cloth clipping bag. The Craftsman logo and "GCV 160" are on the top front of the engine shroud. "Honda" is on the top of the pull cord housing cover. The Craftsman logo is also stamped into the rear discharge chute cover and printed on the sides of the clipping bag. "Dust Blocker" and "EZ Empty Bag" are printed on the top of the clipping bag. The first six numerals of the serial number are the manufacture date in the MMDDYY format. The recalled mowers were manufactured between April 2014 (04xx14) and June 2014 (06xx14). The serial number and model number 384531 are on the data plate on the rear of the mowing deck.
Certain lots of the reagent cartridges show confirmed positive bias averaging 0.4% Hemoglobin A1c units and occasionally up to 1.0% HbA1c units for patient samples when compared to the National Glycohemoglobin Standardization Program (NGSP). QC samples may exhibit a similar bias.
During an FDA inspection it was found that the products are marketed without a cleared 510k.
During an FDA inspection, it was found that the products are being marketed without a cleared 510k.
It has been reported that during use, the SpO2 value displayed on the Hemo Monitor may not update to reflect changes in the patient's oxygen value. It is also possible that if using the pulse rate of the SpO2 finger clip to calculate the patient's heart rate, it too may be subject to displaying a stale value.
Lack of Assurance of Sterility: A small cut in the solution bag may have been introduced during the manufacturing process, resulting in a leak of the bag into the overpouch.
Formulation deviation
Formulation deviation
Positive bias for Calibrator E lot kits ending in 38 and 39 with the ADVIA Centaur Systems Cortisol and Progesterone assays compared to the respective master curves.
Formulation deviation
Formulation deviation
The product was tested and found to be positive for Salmonella.
Internal testing has confirmed a low absorbance range between the levels 1 and 5 calibrators with this lot resulting in the potential for a positive or negative bias and imprecision across the PTN assay range.
The Easy-Care Care-Lock feature installed at the foot of the bed may potentially fail to stay engaged (locked) after the Care-Lock System has been engaged by stepping on the red (locked) pedal.
This recall involves Hearth and Home Technologies®, Heat-N-Glo®, Heatilator®, Outdoor Lifestyles® and Quadra Fire® natural or propane gas indoor and outdoor fireplaces, stoves, inserts and log sets. The following brand names and serial numbers are printed on the unit rating plate, located near the controls, and in the instruction manual. Brand Names Products Serial Numbers Hearth and Home Technologies® Indoor Gas Fireplaces 0023793235 through 0023822923 GA1851161 through GA1851706 Gas Log Sets 0023797015 through 0023812111 1126-3481 and 65174612130 Heat-N-Glo® Indoor Gas Fireplaces, Stoves and Inserts 0023791818 through 0023823238 Heatilator® Indoor Gas Fireplaces and Inserts 0023792110 through 0023823125 0023742749, 0023826583 0023798I69 and 00238012326 Outdoor Lifestyles® Outdoor Gas Fireplaces OD18710 through OD18934 0023792647 through 0023822308 Quadra Fire® Indoor Gas Stoves and Inserts 0023792636 through 0023822725
Mars Chocolate North America is recalling M & Ms due to undeclared peanuts.
GE Healthcare has recently become aware of a potential safety issue to the ECG calculations following a disconnect/reconnect cycle with the Patient Data Module, when used with the Carescape Bx50 monitors. If the PDM is quickly disconnected and reconnected (a less than 10 second cycle) from a Carescape Bx50 monitor following a Patient Discharge or during active monitoring, the ECG waveform an
The external power supply for the Clintek Status analyzer, which is provided separately, is damaged. It can result in an electric shock to the User.