Recalls for 02/23/2021

2022 BLUE BIRD ALL AMERICAN - SEAT BELTS:REAR/OTHER:ANCHORAGE
02/23/2021 Vehicle Recall

Blue Bird Body Company (Blue Bird) is recalling certain 2020-2022 Vision and All American buses. The seats with integrated 3-point seat belts may have been installed incorrectly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 210, "Seat Belt Assembly Anchorages."

  • Company:
    BLUE BIRD
  • Recall Number
    21V070000
2021 FORD BRONCO SPORT - SUSPENSION:FRONT:CONTROL ARM
02/23/2021 Vehicle Recall

Ford Motor Company (Ford) is recalling certain 2021 Bronco Sport vehicles. These vehicles may have been produced with incorrect front lower control arms.

  • Company:
    FORD
  • Recall Number
    21V074000
2014 FORD MUSTANG - AIR BAGS:FRONTAL | AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE | AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
02/23/2021 Vehicle Recall

Ford Motor Company (Ford) is recalling certain 2005-2014 Mustang, 2004-2011 Ranger, 2009-2011 Mercury Milan, 2006 Ford GT, 2008-2012 Fusion, 2007-2010 Edge and Lincoln MKX, and 2009-2010 Lincoln MKZ vehicles. These vehicles may be equipped with a driver or passenger frontal air bag inflator used as a replacement service part, that may explode due to propellant degradation occurring after long-term exposure to high absolute humidity, temperature and temperature cycling.

  • Company:
    MERCURY
  • Recall Number
    21V081000
2014 FORD MUSTANG - AIR BAGS:FRONTAL | AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE | AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
02/23/2021 Vehicle Recall

Ford Motor Company (Ford) is recalling certain 2005-2014 Mustang, 2004-2011 Ranger, 2009-2011 Mercury Milan, 2006 Ford GT, 2008-2012 Fusion, 2007-2010 Edge and Lincoln MKX, and 2009-2010 Lincoln MKZ vehicles. These vehicles may be equipped with a driver or passenger frontal air bag inflator used as a replacement service part, that may explode due to propellant degradation occurring after long-term exposure to high absolute humidity, temperature and temperature cycling.

  • Company:
    LINCOLN
  • Recall Number
    21V081000
2014 FORD MUSTANG - AIR BAGS:FRONTAL | AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE | AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
02/23/2021 Vehicle Recall

Ford Motor Company (Ford) is recalling certain 2005-2014 Mustang, 2004-2011 Ranger, 2009-2011 Mercury Milan, 2006 Ford GT, 2008-2012 Fusion, 2007-2010 Edge and Lincoln MKX, and 2009-2010 Lincoln MKZ vehicles. These vehicles may be equipped with a driver or passenger frontal air bag inflator used as a replacement service part, that may explode due to propellant degradation occurring after long-term exposure to high absolute humidity, temperature and temperature cycling.

  • Company:
    FORD
  • Recall Number
    21V081000
2006 FORD RANGER - AIR BAGS:FRONTAL | AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE | AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
02/23/2021 Vehicle Recall

Ford Motor Company (Ford) is recalling certain 2004-2006 Ranger vehicles that may be equipped with a driver or passenger frontal air bag inflator used as a replacement service part, that may explode due to propellant degradation occurring after long-term exposure to high absolute humidity, temperature and temperature cycling.

  • Company:
    FORD
  • Recall Number
    21V076000
2021 FORD BRONCO SPORT - SUSPENSION:REAR
02/23/2021 Vehicle Recall

Ford Motor Company (Ford) is recalling certain 2021 Bronco Sport vehicles. The rear suspension subframe assembly may have loose or missing bolts.

  • Company:
    FORD
  • Recall Number
    21V075000
Medtronic Announces Voluntary Recall of Unused Valiant Navion™ Thoracic Stent Graft System
02/23/2021 Medical Recall

Medtronic plc , the global leader in medical technology, has voluntarily issued a global recall of unused Medtronic Valiant Navion™ thoracic stent graft system and informed physicians to immediately cease use of the device until further notice.

  • Company:
    Due to endoleaks, stent fractures and stent ring enlargement
  • Problem
    Medical Devices