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All product recalls associated with FOREST RIVER.
Total Recalls
1000
Past Year
1000
Class I (Serious)
145
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.
Forest River, Inc. (Forest River) is recalling certain 2025 Aurora ART26BHS travel trailers. The electrical connector for the air conditioner may have strands of wiring exposed, which can cause electrical arcing.
Identified curing issues with the silicone during the needles manufacturing process.
Identified curing issues with the silicone during the needles manufacturing process.
Identified curing issues with the silicone during the needles manufacturing process.
CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
Defective Container: blister packs not properly sealed resulting in tablets being loose in the carton.
Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
This recall involves the replacement reagent #1 bottles sold with Taylor Phosphate Test Kits #K-1106 and also sold separately. The kits are used to test the level of phosphate in water for pools, spas and aquariums. The water testing kits are labeled with the brand name "Taylor," the kit name "Phosphate Test" and part number "K-1106." The bottle in the kit that contains sulfuric acid is labeled with the brand name "Taylor," product name "Phosphate Reagent #1," part number "R-0980" and "A Size: 22 mL (.75 oz)." The replacement reagent bottle that is sold separately has the same label. Phosphate Reagent #1 has a shelf-life of 24 months.
Jayco, Inc. (Jayco) is recalling certain 2024 Entegra Condor, Jayco Granite Ridge, 2025 Jayco Alante SE, Redhawk SE, and Entegra Odyssey SE motorhomes. The Occupant and Cargo Carrying Capacity (OCCC) on the Federal label may be incorrect and allow the vehicle to be overloaded. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - other than passenger cars."
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
Foreign object (plastic)
Airstream, Inc. (Airstream) is recalling certain 2021-2025 Airstream Classic 33', 2024-2025 Classic 30', and 2025 Classic 28' travel trailers. The sofa footrest switch may have underrated wiring, which can allow the wiring to overheat.
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
Presence of foreign substance: Presence of Benzene.