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All product recalls associated with WHEELED COACH.
Total Recalls
1000
Past Year
590
Class I (Serious)
65
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.
Wheeled Coach Industries (Wheeled Coach) is recalling certain model year 2010 M2, 2013-2014 T1, T2, and T3, and 2014 Terrastar ambulances, equipped with ECX Timer part number EL00230 manufactured by ECX Electronics Corporation. The ECX timer may experience a momentary loss of power when starting the vehicle.
Undeclared milk allergen
Labeling: Missing Label; Three cases of product (total of 36 bottles) were packaged without the primary label on the bottle. The cases were, however, packaged in the correct finished product shipper, labeled with the correct shipper bar code label, sealed with tamper-evident tape and erroneously shipped to Upsher-Smith.
Undeclared milk allergen
Oshkosh Corporation (Oshkosh) is recalling certain model year 2012-2014 S-Series Ready Mixed Concrete trucks manufactured February 29, 2012, through January 27, 2014, and equipped with certain Cummins Westport Model ISL G engines. Condensation in the intake manifold may freeze during cold weather conditions and interfere with the proper operation of the intake manifold pressure sensor.
This recall involves Hussong Manufacturing direct vent gas fireplaces and gas fireplace inserts that use American Flame brand main control modules. There are 22 models sold under the brand names Kozy Heat Fireplaces, Ambiance Fireplaces and Stellar Hearth Products. They were manufactured between October 2009 and April 2013. The fireplace name, model number, manufacture date and serial number are on a silver testing label attached by a chain and next to the gas valve. The following products are being recalled: Model Name (model number) Serial Number Range Mfg. Date Range Month/Year Kozy Heat Chaska (CSK-31-IPI) 10-094223-18 / 12-096088-23 05/10-06/12 Chaska XL (CSK-335-IPI) 10-703738-15 / 12-706417-24 04/10-06/12 Jackson (911-IPI) 10-820097-37 / 12-820636-11 09/10-03/12 Jackson XL (911XL-IPI) 10-9125332-37 / 12-9126288-10 09/10-03/12 Jordan (JOR-30) 10-080001-25 / 12-081992-07 06/10-02/12 Jordan XL (JOR-34) 10-010001-46 / 12-011278-04 11/10-01/12 Minneapolis (MPS-30) 10-080004-25 / 12-081914-02 06/10-01/12 Minneapolis XL (MPS-34) 10-010005-46 / 12-011300-12 11/10-03/12 Rockford (RFD-30) 10-080006-25 / 12-082020-19 06/10-05/12 Rockford XL (RFD-34) 10-010003-46 / 12-011309-12 11/10-03/12 Nicollet (NCL-195) 10-060001-05 / 12-060608-07 02/10-02/12 Dassel (DSL-36-IPI) 10-150789-15 / 12-151789-11 04/10-03/12 Delano (DEL-36-IP I) 10-030001-45 / 12-030908-12 11/10-03/12 Princeton (PRC-3 6-IPI) 09-004528-44 / 12-007203-11 10/09-03/12 Thief River Falls (56701-IP1) 10-242305-15 / 12-245336-12 04/10-03/12 Minnetonka (55345-IPI) 09-407828-30 / 12-411049-11 04/10-04/12 Trimont (TMT-3875-IPI) 10-300771-15 / 12-301183-16 09/11-06/12 Slayton 42 (SLA-42) 11-080012-38 / 12-080402-23 04/10-03/12 Ambiance Intrigue 100 (INT-100) 11-100235-31 / 11-100306-36 04/11-09/11 Intrigue 200 (INT-200) 11-10000-29 / 12-100513-28 07/11-06/12 Stellar Hearth Products Fireplaces CML-58-S (CML-58-S) 10-10006-40 / 13-13021-16 10/10-04/13 CTL-58-S (CTL-58-S) 10-10001-40 / 13-13034-16 10/10-04/13
Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being conducted because the product was given 36 month expiration dates instead of the filed 24 months.
Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being conducted because the product was given 36 month expiration dates instead of the filed 24 months.
Failed Impurity/Degradation Specification; out-of-specification result for one individual unknown impurity at the 24-month room temperature stability test station.
The contract manufacturer has notified Swanson Health Products that Swanson Full Spectrum Cilantro (Coriander) (SW1112) is subject to a recall due to a potential risk of salmonella contamination.
Defective Delivery System: Potential for dose delivery out of specification due to interation of the drug product powder with the lubricant on the interior of the capsule shell.
Products were recalled due to potential Listeria monocytogenes contamination.
Products were recalled due to potential Listeria monocytogenes contamination.
Products were recalled due to potential Listeria monocytogenes contamination.
Superpotent Drug: Product contains twice the stated amount of midazolam.
Products were recalled due to potential Listeria monocytogenes contamination.
Products were recalled due to potential Listeria monocytogenes contamination.
Products were recalled due to potential Listeria monocytogenes contamination.
Products were recalled due to potential Listeria monocytogenes contamination.
Products were recalled due to potential Listeria monocytogenes contamination.