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All product recalls associated with DANA.
Total Recalls
22
Past Year
0
Class I (Serious)
0
Most Recent
Jun 2024
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.
Dana Incorporated (Dana) is recalling certain D-Series and E-Series Steer Axles, and replacement tie rod assemblies for Dana D-Series and E-Series Steer Axles. The tie rod assemblies in these steer axles contain ball studs that may have been incorrectly heat-treated, which can cause them to break, and possibly result in tie rod failure.
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Dana Incorporated (Dana) is recalling certain Heavy Vehicle Output shafts, part number 131536, used in drive axles manufactured for commercial vehicles. The output shafts may not have been properly heat treated, which can cause the shaft to fracture at the transition of the shaft splines to the thread, allowing the shaft or the interaxle driveline to detach from the vehicle.
Undeclared sulfites in product label.
Undeclared sulfites in product label.
Dana Driveshaft Manufacturing, LLC (Dana) is recalling certain commercial vehicle lightweight driveshafts, model SPL250, sizes 1610-2200 or 2220-2830, manufactured January 2, 2013, through June 30, 2013. In affected driveshafts, the welded bond of the driveshaft and the rear yoke may fail, leading to slippage between the driveshaft and yoke and, potentially, to loss of torque to the rear wheels.
Dana Driveshaft Manufacturing, LLC (Dana) is recalling certain commercial vehicle lightweight driveshafts, model SPL250. In affected driveshafts, the welded bond of the driveshaft and the rear yoke may fail, leading to slippage between the driveshaft and yoke and, potentially, to loss of torque to the rear wheels.
This recall includes 14 models of PT Domusindo Perdana wooden drop-side cribs. The name, model number and date codes are printed on the plywood mattress board. Model # Description Date Code 343-1509 Jenny Lind Crib 01/1991-12/1997151 343-3810 Christopher Crib 2001151 343-5500 Early American Crib 01/1998-12/1999151 343-6771 Scottsdale Crib 01/1998/12/1999151 343-7100 Sleigh Crib without Rosette 01/2004-12/2006 343-7134 Sleigh Crib 01/2001-2/2004 343-7144 Anniversary Sleigh Crib 01/2002-12/2004 343-7753 Kristin Crib 01/1998-12/1999 343-8249 Cameron Crib 01/1998/12/1999 343-8020 Solid Panel Sleigh Crib 01/2001-12/2002 343-8070 Roll Bar Convertible Crib 01/2004-12/2005 343-8155 Anniversary ConvertibleSleigh Crib 01/2002-12/2006 343-8200 Spindle Convertible Crib 01/2001-12/2005 343-8913 Bella 3-in-1 Crib 01/2005-12/2008
Sold under the brand names Architectural Audio and HomeTech, these in-wall volume controls were professionally installed as part of whole house audio systems. The switch plate covers for the recalled systems are white or almond, and "aVc" (amplified volume control) is imprinted above the volume control. They have the following model numbers: Brand Model Numbers Architectural Audio 20127 20128 HomeTech 10114 10115 The model number is not visible to the consumer, and consumers are instructed not to remove the keypads from the wall to look for a model number. All serial numbers are included in the recall.
There is a switch malfunction that that may cause the unit not to respond when command key is depressed.
This prescription device, without an approved 510K , was distributed to unauthorized consumers, mostly pregnant women, on the internet.