Forest River Recalls 2017-2019 Crossfit Coaches for Incorrect Weight Placards
Forest River is recalling 2017-2019 Crossfit coaches because incorrect weight placards may lead to vehicle overloading and increased crash risk.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (vehicle overloading leading to crash risk) where injury has not yet been reported, fitting the High severity criteria.
Plain-English summary
Forest River, Inc. is recalling certain 2017-2019 Coachmen Crossfit vehicles. The Federal Placards on these vehicles incorrectly list a rear axle Gross Axle Weight Rating (GAWR) that exceeds the GAWR assigned by the chassis manufacturer.
The incorrect GAWR may cause the operator to overload the vehicle, increasing the risk of a crash. No specific injuries or fatalities are reported in the source text.
Forest River has notified owners and provided a corrected Federal Placard free of charge. The recall began on April 25, 2018. Owners may contact Forest River customer service at 1-574-825-8590 or the NHTSA Vehicle Safety Hotline at 1-888-327-4236.
The recalled product
- Product
- FOREST RIVER CROSSFIT
- Brand
- FOREST RIVER
- Manufacturer
- Forest River, Inc.
- Category
- Vehicle — Recreational Vehicle
- Hazard
- Affected units
- 201
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Model numbers (1)
- CROSSFIT
Distribution
Distributed nationwide across the United States.
Related recalls
Same brand · FOREST RIVER
- HighForest River Recalls 2027 Vibe Trailers Due to Carbon Monoxide Risk
NHTSA · 2026-09-01
- HighForest River Recalls 2027 Freelander and Leprechaun RVs for Fire Risk
NHTSA · 2026-08-03
- High
- HighForest River Recalls 2026-2027 Pause and OG Luxury Coaches for Fire Risk
NHTSA · 2026-07-23
- High
Same manufacturer · Forest River, Inc.
See all →- High
- High
Same hazard · mis labeling
See all →- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- HighByron White A-L Complex Herbal Supplement Recalled for Undeclared Walnut
FDA (Food) · 2026-09-02
- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02