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All product recalls associated with COACHMEN.
Total Recalls
1000
Past Year
899
Class I (Serious)
125
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 Coachmen Catalina BCAT154RBX travel trailers. The wastewater holding tank pipe may not extend to the exterior of the vehicle, allowing sewer gas to enter the cabin.
Field action to clarify the flow rates and inlet fluid temperatures, along with location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets.
Forest River, Inc. (Forest River) is recalling certain 2025 Coachmen Brookstone BKF398MBL fifth wheels. The wastewater holding tank pipe may not extend to the exterior of the vehicle, allowing sewer gas to enter the cabin.
Patient monitor has nine identified cybersecurity vulnerabilities.
The high voltage capacitor may fail early in the product life cycle after delivery of surge voltages. When this failure occurs, the capacitor may produce smoke and a burning smell. In extremely rare instances a capacitor may cause a spark or excessive heat when an internal capacitor failure occurs.
Due to a software issue, the software may incorrectly process the date of birth (DoB) received from the Laboratory Information System (LIS) and when the DoB is set to 01/01/1900 or left empty, REMISOL Advance may incorrectly identify a patient as a newborn, affecting the execution of validation rules based on incorrect reference ranges. The test results are not changed by this software defect and are accurately displayed by REMISOL Advance; however, the evaluation flagging of the results may be affected. This issue may lead to wrong reference range calculations and can result in erroneous flagged results being auto validated and uploaded to LIS.
Vials of implant bone granules may contain less product then specified on labeling.
Apic Yamada has recently discovered that certain products may be out of compliance with FDA electronic product regulations in that they did not bear a required label.
Product mislabeled - product labeled as peanuts, but may contain cashews
Potential for internal fastening mechanism within generator of mobile x-Ray to fail.
Potential for microbial contamination.
Forest River, Inc. (Forest River) is recalling certain 2025 Coachmen Apex and Remote travel trailers. The solar panel wiring may be incorrectly wired to the battery, causing it to melt.
Potential for microbial contamination.
Preset treatment parameters are not consistently being used in accordance with the IFU.
Undeclared allergen (soy)
This recall involves Ashland 10-inch and 14-inch two-bar right-hand and left-hand casement window hinge tracks installed in windows to allow the windows to be cranked opened and closed. The casement window hinge tracks include part numbers 2003558, 2003559, 2004271 and 2004272. These products can be identified by locating "R10," "L10," "R14" or "L14" located on the face of the casement window hinge track. These hinge tracks were manufactured and sold to residential and commercial window manufacturers in boxes dated April 2024 through December 2024.
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
Evaluation handsets may not be able to communicate with the neurostimulator due to handsets having a faster processing speed than prior handsets. An inability to connect may cause the therapy to stop being delivered and a system error will be displayed. Patient may experience return of underlying disease symptoms (e.g. overactive bladder, urinary retention, or fecal incontinence) based on their response to stimulation during the evaluation period.
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.