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All product recalls associated with HOST CAMPERS.
Total Recalls
1000
Past Year
1000
Class I (Serious)
143
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.
HOST INDUSTRIES (Host) is recalling certain 2022-2025 Host Mammoth, Yukon, Cascade, Tahoe, and Everest trailers. The LED backlight circuit board in the cooktop range may fail, causing the board to overheat.
Forest River, Inc. (Forest River) is recalling certain 2024 Forest River Rainier, Stealth Evo, Salem, Vibe, and Wildwood travel trailers. The tire may contact the vehicle body due to insufficient clearance, which can cause tire damage.
Expired Products distributed to customers
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
Queso fresco was found to contain Listeria monocytogenes.
Potential issue causing a higher frequency of interference with locking screws and/or inserter rods than anticipated, resulting in screws stripping and/or not fully seating in the plates and/or interface issues between inserter rods and plates.
Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.
There is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) settings.
Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.
Thermo King Corp. (Thermo King) is recalling certain Tripac-3 Auxiliary Power Units (APU) with part number 800908, manufactured between April 8, 2024, and May 15, 2024. The APU mounting kits contain mounting bolts that are too short and can loosen.
Smiths Medical became aware of an issue related to a potential for the patient outlet connector to loosen/detach from the paraPAC Plus P300 and P310 ventilators impacting the active ventilation function.
Difficulties in pairing the wireless footswitch with the Soltive Laser, potentially delaying the surgical procedure.
Smiths Medical became aware of an issue related to a potential for the patient outlet connector to loosen/detach from the paraPAC Plus P300 and P310 ventilators impacting the active ventilation function.
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
Issue with analyzer when the pH of the calibration solution decreases during the in-use period potentially because of bacterial growth in the calibration solution bottles. This may result in a probability of reporting biased out-of-specification pH results on blood samples.
There is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) settings.
Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C.
Tip holder portion of the scaler tip assembly may have an oversized condition that will not allow the scaler tip to stay seated in the holder may cause injury
Potential of the handset plug to disconnect from the nebulizer port on the blue ventilator adapter. The handset plug is required to ensure proper operation and ventilator gas flow.