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All product recalls associated with THOR MOTOR COACH.
Total Recalls
1000
Past Year
589
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.
Thor Motor Coach (TMC) is recalling certain 2021 Four Winds motorhomes, equipped with Dometic 3 burner cooking stoves. The saddle valve securing bolt may be overtightened, possibly damaging the o-ring seal and causing a continuous gas leak.
A software defect that has the potential to result in image misdiagnosis and incorrect treatment of a patient.
Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the display of a Speaker Malfunct. INOP or by the absence of audible sound, may result in delayed treatment of the patient.
Marketed without an Approved NDA/ANDA: Product marketed with drug claims.
Failed Dissolution Specifications: Out of specification for dissolution.
Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the display of a Speaker Malfunct. INOP or by the absence of audible sound, may result in delayed treatment of the patient.
Product contain undeclared milk.
Products contain undeclared milk and Uranine-Acid Yellow 73
Thor Motor Coach (TMC) is recalling certain 2020-2021 Daybreak, Four Winds, Chateau, Freedom Elite, Quantum motorhomes built on a Chevrolet chassis. The BIM (Battery Isolation Manager)/BIR (Battery Isolation Relay) is not watertight when exposed to engine compartment heat.
A software error was detected within software version 1.3.4 for the Tempus LS device. When exiting pacer back into manual mode the pacer pulse wave may put the ECG calibration out of calibration. This software error may result in a delay in therapy, as the clinician is not provided an ECG waveform on which a shockable rhythm decision can be made. The device is still able to deliver a manual defibrillation shock.
The firm is recalling their products due the unapproved use of a food additive and unapproved marketing statements
Under rare circumstances, the component may be susceptible to a failure mechanism that could impact device performance, including potential loss of function.
Under rare circumstances, the component may be susceptible to a failure mechanism that could impact device performance, including potential loss of function.
Under rare circumstances, the component may be susceptible to a failure mechanism that could impact device performance, including potential loss of function.
This recall involves InvoSpa electric throw heated blankets. The recalled blankets measure 50 inches by 60 inches. The blankets are made of silky flannel and sherpa shu velveteen and are white and gray. Model number ML-G03 and InvoSpa are printed on a tag on the blanket.
Two issues were found with the treatment plan report: 1) There may be incorrect information for the percent of a region of interest with a clinical goal that is outside the dose grid; and 2) For RayStation and RayPlan 9B and 10A, 6D couch angles may be incorrect.
Failed Impurities/Degradation Specifications: One lot of Levocetirizine dihydrochloride tablets 5 mg 30 count failed stability testing.
Potential for no-flow and leaks under the twist clamp.
Potential Salmonella contamination.
During system upgrade incorrect comments may be added to existing tests. In such instance: Resting ECG and ABP tests which did not contain comments at the time of the upgrade, may have unrelated comments added. Existing comments will not be overwritten or removed. Rhythm ECG Tests may have comments overwritten with unrelated comments. Any tests created after the upgrade are not affected.