Loading...
Loading...
All product recalls associated with Abbott Molecular.
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.
Thermal runaway conditions, in that the target temperature was exceeded and the temperature display could not track the actual temperature within the heated slide basins of the VP 2000 Slide Processor.
Product labeled as 4 mm High Viscosity Injector tip contains a 6 mm tip.
Leak, disposal bag: A Merit Disposal Depot (MDD) bag contained in certain custom waste management kits may leak. For further information, please contact Merit Medical Systems, Inc. by telephone at 801-208-4748.
Difficulty inserting guidewire through introducer needle. Needle hub is not tapered down to the needle cannula.
Multiprint report may contain incorrect vital data for patients
The C-arm rotation brake does not always function properly, and may not hold the C-arm position if the C-arm is not positioned in its maximum rotation and if it is accidentally bumped by medical staff or patients. Unwanted C-arm movement may cause the C-arm to collide with a patient. The brakes function properly if the C-arm is rotated to its maximum positions.
The C-arm rotation brake does not always function properly, and may not hold the C-arm position if the C-arm is not positioned in its maximum rotation and if it is accidentally bumped by medical staff or patients. Unwanted C-arm movement may cause the C-arm to collide with a patient. The brakes function properly if the C-arm is rotated to its maximum positions.
The front protective cover may loosen and completely fall off.
No 510k approved
There is a possibility for misregistration when brain scans are performed with Infinia with the Hawkeye option. This misregistration could present the potential for misdiagnosis when the patient headrest sags under the weight of a head.
The firm found that for this particular lot that the barcode, used for entering the characteristics of CAL1 Solution into the analyzer, does not reflect the actual values of the solution. As a consequence, the calibration curves for these parameters and thereby the measured results for patient samples and quality controls will be biased.
Reliability of the Stand-Trolley cable may result in loss of images on the monitor during an examination. This intermittent problem can lead to System lock-up, where no radiation is possible and images are not visible on the monitor
Reliability of the Stand-Trolley cable may result in loss of images on the monitor during an examination. This intermittent problem can lead to System lock-up, where no radiation is possible and images are not visible on the monitor
Some units of Fluro-Ethyl containing the defective valve which could malfunction and spray refrigerant out from the side of the valve in addition to or instead of spraying in the normal inverted position from the product's actuator. The product can also leak coolant from the side of the valve onto the fingers of the user.
The recall involves bicycles with Deda Forza black carbon fiber handlebar stems in gloss finish. "Deda Forza" is printed on the handlebar stem. Deda Forza black carbon fiber handlebar stems in matte finish are not included in this recall.
This recall involves the following Wolf Appliance 48-Inch gas ranges with model numbers: P48, PS48 and R48. The gas ranges are stainless steel with a double oven. A "Wolf" appliance logo is on the front of the larger oven door.
The recalled carriers were sold under the "Action Baby Carrier" brand name. The carriers are sold in various colors and patterns: blue, brown, green, "so square", "the larrisa" and "spring breeze."
The cotton knit sweaters are cream colored with a blue stripe at the wrists and waist, a blue ball on the hood, and blue buttons. There is a drawstring through the hood with pom-poms at the ends. The sweaters were sold in children's size 2T under the brand name "Empress Arts." "Empress Baby" is sewn into the sweater's tag.
GE Healthcare has found that the sterile products manufactured by Contour Fabricators, Inc. (CFI) for GE healthcare (GEHC) may have sterile seals that could be compromised during the shelf life of the products. This issue could result in the product not maintaining its sterile state.
Two defects have been identified: 1) potential to display a patient on the canvas page that is different from the patient whose images are displayed on diagnostic monitors when using Conference Presentation States and when opening two or more studies from a folder or an exam worklist and 2) potential to miscalculate measurements when Pixel Spacing and Imager Pixel Spacing DICOM tag values are bot