Loading...
Loading...
All product recalls associated with CATERPILLAR.
Total Recalls
1000
Past Year
123
Class I (Serious)
69
Most Recent
Nov 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.
Caterpillar Inc. (Caterpillar) is recalling certain model year 2015 CT660, and CT681 trucks manufactured July 28, 2014, to November 5, 2014. The affected vehicles may experience brake drag due to an improperly seated diaphragm in the brake chamber.
Elevated brand ice cream products are being recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain ice cream mix produced and recalled by Snoqualmie Gourmet Ice Cream
Elevated brand ice cream products are being recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain ice cream mix produced and recalled by Snoqualmie Gourmet Ice Cream
Elevated brand ice cream products are being recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain ice cream mix produced and recalled by Snoqualmie Gourmet Ice Cream
Elevated brand ice cream products are being recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain ice cream mix produced and recalled by Snoqualmie Gourmet Ice Cream
Elevated brand ice cream products are being recalled due to the potential to be contaminated with Listeria monocytogenes. These products contain ice cream mix produced and recalled by Snoqualmie Gourmet Ice Cream
Labeling: Illegible Label: Sandoz Inc. is recalling of one lot of Fluoxetine Capsules due to an illegible logo on the capsule.
Golden Chocolate International, Inc. has recalled (3) products due to the use of undeclared FD&C Yellow #5, FD&C Yellow #6, and FD&C Red #40 food colorings.
Golden Chocolate International, Inc. has recalled (3) products due to the use of undeclared FD&C Yellow #5, FD&C Yellow #6, and FD&C Red #40 food colorings.
Golden Chocolate International, Inc. has recalled (3) products due to the use of undeclared FD&C Yellow #5, FD&C Yellow #6, and FD&C Red #40 food colorings.
Accuray has become aware of a potential safety issue related to the TomoTherapy Treatment System caused by a failure to monitor the jaw position after a jaw error occurs. This may result in an incorrect jaw position during treatment, without generating system interruption.
Replacement LED Board kit of Natus neoBLUE2 Phototherapy system distributed after February 16, 2012 is subject of a Field Safety Notification because the system will exhibit a higher light intensity output than the original device. While some customers may prefer using these lights at the higher intensity levels, some are concerned that patients may receive more intensity than desired.
Customer notification that the device may be difficult to open or close.
Software upgrade to correct potential safety issue related to CyberKnife System that occurs when upgrading the Treatment Delivery Software for the first generation Iris Variable Aperture Collimator.
Product may contain mold.
This recall involves Waterway Plastics Designer Pro Series suction covers with model number 640-52XX S, printed on top of the outside edge of the plastic. The round covers are black and silver and were installed in select spas manufactured by Catalina Spas, Four Winds Spas, Dimension One Spas, and Sunrise Spas from June 2011 to June 2013. The covers are installed on the following model spas: Sunrise Spas Series 989 Aquarian, Bimini (Mermaid brand only), 939 Endeavour, 959 Equinox, Essence 250, Genesis 250, Jewel 250, Legend 250, Medallion 350, S102 (Whitewater brand only), S103, S104, S105, 203LS, 204LS, 205LS, 949 Meridian, 249 Spirit SE, Tonga (Mermaid brand only). Model and series numbers are located on the cabinet panel on the lower right side near the top side control. Dimension One Spa Series At Home Series, Bay Series, Reflection Series and Streamline spas The model name is on the inside of the cabinet access door. Four Winds Spa Series XL Swim Spas XL 12000, XL14000, XL 16000 The model name is printed on stainless steel plates mounted on the outside of the spa. They are usually located on the left panel, using the topside as the front panel. Catalina Spas All models manufactured from 2011-2013.
All packages of Falope Ring Band Applicator kits are being recalled due to compromises in sterile packaging that could be associated with bacterial contamination that might lead to patient infection.
Failed Impurities/Degradation Specifications : Out-of-specification result for an unidentified impurity at the 12 month stability test point.
The box of guides for a specific case arrived intact but contained two (2) femoral guides instead of one (1) femoral guide and one (1) tibial guide. The device did not meet specification: One tibia guide missing and one femur guide contained an edge which was +0.04 mm over specification.
When not used correctly, Accusorb MRI products may overheat and lead to patient injury.