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All product recalls associated with COACHMEN.
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.
Forest River, Inc. (Forest River) is recalling certain 2024 Coachmen Brookstone, Chaparral, Chaparral Lite, and Shasta Phoenix fifth wheel trailers. The affected vehicles may have been manufactured with an incorrect fuse in the power distribution center.
Forest River, Inc. (Forest River) is recalling certain 2021-2024 Coachmen Prism and 2023-2024 Coachmen Concord vehicles. The Federal Placard may indicate incorrect information about the number of seat belts.
A sterilization nonconformance prematurely aged the product, resulting in an inaccurate labeled expiration date.
This recall involves Zevo Fly, Gnat and Fruit Fly Flying Insect Killer3 Value Packs. The twin pack aerosol containers are shrink-wrapped together with a white and purple label. The batch code 3045D185EW3 is printed on the bottom of the aerosol containers or on the shrink-wrap. "Zevo Insect Killer" and "Fly, Gnat & Fruit Fly" and "Kills on Contact" are printed on the shrink-wrap.
This recall involves certain VINs of Model Year 2023 Polaris RANGER XP 1000 / XP 1000 Crew, RANGER 1000 / 1000 Crew and Model Year 2024 Polaris Pro XD Full-Size Diesel Crew, Model Year 2024 Gravely ATLAS JSV-3400 and Model Year 2024 Bobcat UV34XL Gas off road vehicles. The RANGER vehicles were sold in the following colors: blue, graphite, camouflage, brown and white. The Pro XD vehicles have gray plastic body panels with a black frame/accents. The RANGER vehicles were sold in three- and six-seat configurations. The Pro XD, Gravely and Bobcat vehicles have two or four seats. The RANGER and Pro XD vehicles have "POLARIS" stamped on the front grille, the Gravely vehicles have "Gravely" stamped on the front grille and the Bobcat vehicles have the Bobcat logo on the front grille.
Chrysler (FCA US, LLC) is recalling certain 2022-2023 Ram 1500, Ram 3500 Cab Chassis with GVWR less than 10,000 lbs., and 2022-2024 Ram 2500 vehicles. The radio software may prevent the rearview image from displaying. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility."
Diamond C Trailer MFG. (Diamond C) is recalling certain 2023-2024 FMAX, SDX, and PX trailers equipped with a spare tire winch. The winch system that secures the spare tire to the trailer may loosen or fail over time.
FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.
Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention.
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention.
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention.
Affected lots of product may experience technical distortions to a greater extent than expected.
Affected lots of product may experience technical distortions to a greater extent than expected.
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention.
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication. There is also the potential for life-threatening situations to occur requiring additional medical intervention.
Specific serial numbers of GraftonTM DBM product due to the potential that a step during the inspection of the outer Tyvek pouch may not have been performed according to requirements. Based on this, batches may have been released with potential non-conformances in the outer Tyvek pouch.