Recalls
Submitted by legality on Wed, 02/04/2009 - 18:30.
Update
NHTSA Campaign ID Number: 09T007
Synopsis:
Bridgestone Americas Tire Operations, LLC (BATO) is recalling 127,183 Firestone FR380 tires, size P235/75R15, manufactured from September 9, 2007 through July 2, 2008. These tires were produced with insufficient tread base gauge. Continued use of the subject tires may lead to vibration and groove cracking. Extended use could lead to tread distortion or tread separation and loss of vehicle control. BATO will notify owners and replace the affected tires free of charge. BATO will also mount and balance the replacement tires, all at no charge or expense to the owner. The safety recall is expected to begin on or about June 29, 2009. Owners may contact BATO toll-free at 1-800-465-1904 or visit their website at www.firestonetire.com.
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Please click on the following NHTSA Campaign ID links to view the recall information.
NHTSA Campaign ID Number : 09V174
MAKE / MODEL YEARS :
HONDA / 2008
SUBJECT : HOSE CLAMP FAILURE CAUSING COOLANT LEAK
NHTSA Campaign ID Number : 09V173
MAKE / MODEL YEARS :
VOLVO / 2001-2008
SUBJECT : WIPER MOTOR
NHTSA Campaign ID Number : 09V172
MAKE / MODEL YEARS :
PONTIAC / 2008-2009
SUBJECT : TPMS & BRAKE PEDAL POSITION SWITCH/FMVSS 138 & 108
NHTSA Campaign ID Number : 09V171
MAKE / MODEL YEARS :
HYUNDAI / 2002-2003
SUBJECT : INTERIOR DOOR HANDLE LACERATION /GOLD INDUSTRIES
NHTSA Campaign ID Number : 09V170
MAKE / MODEL YEARS :
DUCATI / 2009-2010
SUBJECT : FUEL LINE ASSEMBLY REPLACEMENT
NHTSA Campaign ID Number : 09V169
MAKE / MODEL YEARS :
NISSAN / 2003-2007
SUBJECT : INTAKE AIR DUCTS/RESONATOR
NHTSA Campaign ID Number : 09V168
MAKE / MODEL YEARS :
TEREX / 1999-2001
SUBJECT : AERIAL UNITS/LIFT CYLINDER FAILURE
NHTSA Campaign ID Number : 09V167
MAKE / MODEL YEARS :
AUTOCAR / 2008-2009
SUBJECT : PARK BRAKE RESET PRESSURE
NHTSA Campaign ID Number : 09V166
MAKE / MODEL YEARS :
KENWORTH / 2005,2007-2009
SUBJECT : AIR DISC BRAKE CALIPER MOUNTING FASTENERS/BENDIX
NHTSA Campaign ID Number : 09V165
MAKE / MODEL YEARS :
KENWORTH / 2008
SUBJECT : VAIABLE VALVE ACTUATION OIL LINE/CATERPILLAR
NHTSA Campaign ID Number : 09V164
MAKE / MODEL YEARS :
VOLKSWAGEN / 2006-2009
SUBJECT : DRIVESHAFT SCREWS
NHTSA Campaign ID Number : 09V163
MAKE / MODEL YEARS :
FLEETWOOD / 2009
SUBJECT : FEDERAL CERTIFICATION TAGS/PART 567 CERTIFICATION
NHTSA Campaign ID Number : 09V161
MAKE / MODEL YEARS :
JAGUAR / 2007-2009
SUBJECT : TPMS FAILURE TO DISPLAY WARNING/FMVSS 138
NHTSA Campaign ID Number : 09V160
MAKE / MODEL YEARS :
DUCATI / 2008
SUBJECT : MAIN WIRING HARNESS ROUTING
NHTSA Campaign ID Number : 09V156
MAKE / MODEL YEARS :
PETERSEN / 1998-2009
SUBJECT : SPINDLE FAILURE
Thank you,
Recalls Subscription Team
Office of Defects Investigation (ODI)
National Highway Traffic Safety Administration (NHTSA)
U.S. Department of Transportation (DOT)
Please click on the following NHTSA Campaign ID links to view the recall information.
NHTSA Campaign ID Number : 09V174
MAKE / MODEL YEARS :
HONDA / 2008
SUBJECT : HOSE CLAMP FAILURE CAUSING COOLANT LEAK
NHTSA Campaign ID Number : 09V173
MAKE / MODEL YEARS :
VOLVO / 2001-2008
SUBJECT : WIPER MOTOR
NHTSA Campaign ID Number : 09V172
MAKE / MODEL YEARS :
PONTIAC / 2008-2009
SUBJECT : TPMS & BRAKE PEDAL POSITION SWITCH/FMVSS 138 & 108
NHTSA Campaign ID Number : 09V171
MAKE / MODEL YEARS :
HYUNDAI / 2002-2003
SUBJECT : INTERIOR DOOR HANDLE LACERATION /GOLD INDUSTRIES
NHTSA Campaign ID Number : 09V170
MAKE / MODEL YEARS :
DUCATI / 2009-2010
SUBJECT : FUEL LINE ASSEMBLY REPLACEMENT
NHTSA Campaign ID Number : 09V169
MAKE / MODEL YEARS :
NISSAN / 2003-2007
SUBJECT : INTAKE AIR DUCTS/RESONATOR
NHTSA Campaign ID Number : 09V168
MAKE / MODEL YEARS :
TEREX / 1999-2001
SUBJECT : AERIAL UNITS/LIFT CYLINDER FAILURE
NHTSA Campaign ID Number : 09V167
MAKE / MODEL YEARS :
AUTOCAR / 2008-2009
SUBJECT : PARK BRAKE RESET PRESSURE
NHTSA Campaign ID Number : 09V166
MAKE / MODEL YEARS :
KENWORTH / 2005,2007-2009
SUBJECT : AIR DISC BRAKE CALIPER MOUNTING FASTENERS/BENDIX
NHTSA Campaign ID Number : 09V165
MAKE / MODEL YEARS :
KENWORTH / 2008
SUBJECT : VAIABLE VALVE ACTUATION OIL LINE/CATERPILLAR
NHTSA Campaign ID Number : 09V164
MAKE / MODEL YEARS :
VOLKSWAGEN / 2006-2009
SUBJECT : DRIVESHAFT SCREWS
NHTSA Campaign ID Number : 09V163
MAKE / MODEL YEARS :
FLEETWOOD / 2009
SUBJECT : FEDERAL CERTIFICATION TAGS/PART 567 CERTIFICATION
NHTSA Campaign ID Number : 09V161
MAKE / MODEL YEARS :
JAGUAR / 2007-2009
SUBJECT : TPMS FAILURE TO DISPLAY WARNING/FMVSS 138
NHTSA Campaign ID Number : 09V160
MAKE / MODEL YEARS :
DUCATI / 2008
SUBJECT : MAIN WIRING HARNESS ROUTING
NHTSA Campaign ID Number : 09V156
MAKE / MODEL YEARS :
PETERSEN / 1998-2009
SUBJECT : SPINDLE FAILURE
Thank you,
Recalls Subscription Team
Office of Defects Investigation (ODI)
National Highway Traffic Safety Administration (NHTSA)
U.S. Department of Transportation (DOT)
5-25-09
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AS Medications Solution LLC. Announces a Nationwide Recall of All Lots of Digoxin Tablets 0.25mg Due to Size Variability (May 11)
Tue, 12 May 2009 14:09:00 -0500
A S Medication Solutions, LLC, a drug repackage company, announced today that all tablets of Caraco brand Digoxin, USP, 0.25 mg, distributed prior to March 31, 2009, which are not expired and are within the expiration date of August, 2011, are being voluntarily recalled to the consumer level. The tablets are being recalled because they may differ in size and therefore could have more or less of the active ingredient, digoxin.
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FDA Alerts Consumers to Recall of Certain Pistachios (March 30)
Mon, 30 Mar 2009 18:59:00 -0500
The FDA and the California Department of Public Health (CDPH) are investigating Salmonella contamination in pistachio products sold by Setton Pistachio of Terra Bella Inc, Calif. The company has stopped all distribution of processed pistachios and will issue a voluntary recall involving approximately 1 million pounds of its products.
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Aqua Star Issues Allergy Alert on Undeclared Peanut In Shrimp Appetizer (February 6)
Sat, 07 Feb 2009 10:30:00 -0600 FDA
Aqua Star of Seattle, WA is recalling Shrimp Appetizers (13.5 oz), because it may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life threatening allergic reaction if they consume this product. None of the peanuts in this product are associated with the nationwide recall of salmonella contaminated peanut butter.
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Ther-Rx Corporation Issues Voluntary Nationwide Recall Of Prescription Prenatal and Iron Supplements To Wholesale Level (February 3)
Wed, 04 Feb 2009 06:51:00 -0600 FDA
Ther-Rx Corporation, a subsidiary of KV Pharmaceutical Company is issuing a voluntary nationwide recall of prescription prenatal and iron supplement nutritionals as identified below (all lots within their expiration dates) at a wholesale level. The Company is taking this action as a precautionary measure, because the products may have been manufactured under conditions that did not sufficiently comply with current Good Manufacturing Practice (cGMP).
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California Firm Recalls Chicken Bouillon Products Imported From an Unapproved Source
Tue, 24 Feb 2009 19:25:36 -0600 USDA
Wei-Chuan USA, Inc., a Bell Gardens, Calif., establishment, is recalling approximately 89,531 pounds of granulated chicken bouillon products that were ineligible for import to the U.S.
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Medical Device Recalls - Hill-Rom 70 Semi-Electric Bed (Class 2 Recall)
Hill-Rom 70 Semi-Electric Bed, Model HS-968 has been recalled. This is a general purpose bed for use with low to medium acuity patients in the home care environment… FDA 2-27-09
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Marron Foods Recalls Instant Non Fat Dry Milk Boxes That May Contain Foreign Material (February 27)
Sun, 01 Mar 2009 17:10:00 -0600
Product was distributed in Safeway Food stores nationally.
FDA
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Goya Foods, Inc. Announces Voluntary Recall of Dried Yellow Potato (Papa Seca Amarilla) (February 27)
Fri, 27 Feb 2009 17:45:00 -0600 FDA
Goya Foods, Inc. of Secaucus, NJ, is recalling its 12 ounce packages of Dried Yellow Potato (Papa Seca Amarilla), UPC 041331050562, because it contains undeclared sulfites. Consumers who have sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
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There is a safety recall regarding Child Restraint Systems from NHTSA's Office of Defects Investigation. 3-4-09
NHTSA Campaign ID Number: 09C002
Synopsis:
RECARO North America, Inc. is recalling certain Signo child restraint assemblies manufactured from Februay through September 2008. The central front adjuster strap on some seats may slip within the metal adjuster (A-Lock) that controls tightness of the harness, thereby preventing the harness from being properly tightened. If this condition existed and a vehicle crash occurred, the child would not be properly secured in their child restraint system and may sustain injury. RECARO will notify owners and replace any defective child restraint system free of charge. The recall is expected to begin during March 2009. Owners can contact RECARO customer service toll-free at 1-888-473-2290.
For more information for this particular recall, please go to 09C002.
There is a safety recall regarding Vehicles from NHTSA's Office of Defects Investigation. 3-23-09
Please click on the following NHTSA Campaign ID links to view the recall information:
NHTSA Campaign ID Number : 09V090
MAKE / MODEL YEARS :
S&S / 2004-2007
SUBJECT : REFRIGERATOR/DOMETIC
NHTSA Campaign ID Number : 09V089
MAKE / MODEL YEARS :
TRIPLE E RV / 2004-2007
SUBJECT : REFRIGERATOR/DOMETIC
NHTSA Campaign ID Number : 09V088
MAKE / MODEL YEARS :
BMW / 2008
SUBJECT : FRONT AXLE SHAFT
NHTSA Campaign ID Number : 09V087
MAKE / MODEL YEARS :
STERLING / 2008-2009
SUBJECT : AFTERTREATMENT REGENERATION DEVICE BODY/CATERPILLA
NHTSA Campaign ID Number : 09V085
MAKE / MODEL YEARS :
FLEETWOOD / 2009
SUBJECT : INCORRECT CERTIFICATION LABEL/PART 567
NHTSA Campaign ID Number : 09V084
MAKE / MODEL YEARS :
DODGE / 2008-2009
SUBJECT : WINDSHIELD WIPER MODULE MOTOR/PART 567
NHTSA Campaign ID Number : 09V082
MAKE / MODEL YEARS :
DODGE / 2009
SUBJECT : ELECTRICAL CONNECTOR
NHTSA Campaign ID Number : 09V081
MAKE / MODEL YEARS :
MERCEDES BENZ / 2009
SUBJECT : DOOR LOCKS
NHTSA Campaign ID Number : 09V079
MAKE / MODEL YEARS :
LONG CHI / 2005-2008
LONG CHIH / 2005-2008
SUBJECT : TIRE PLACARD LABEL/FMVSS 110/LONG CHIH
Recalls Subscription Team
Office of Defects Investigation (ODI)
National Highway Traffic Safety Administration (NHTSA)
U.S. Department of Transportation (DOT)
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The Shiley 3.0PED Cuffless Pediatric Tracheostomy Tube has been recalled by Covidien Inc. because it may be difficult to insert.
FDA notified healthcare professionals of a Class 1 Recall of specific lots due to complaints received about difficulty inserting: 1) the device used to place the tracheostomy tube into the windpipe (obturator), and/or 2) a suction tube (catheter) into the tracheostomy tube. This problem may require that the tracheostomy tube be removed and replaced. Healthcare professionals and hospitals should remove all remaining affected products from their inventory, and return them for replacement or credit.
3-10-09
Read the MedWatch safety summary, including a link to the Recall Notice, at:
http://www.fda.gov/medwatch/safety/2009/safety09.htm#Shiley
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FDA notified healthcare professionals of a Class 1 Recall of model numbers Mono 2M8151 and 2M8153, CX 2M8161 and 2M8163, and CXE 2M9161and 2M9163. These products were manufactured and distributed from February, 1997 through December, 2008. The company identified software and battery usage failures that result in a delay in or interruption of infusion that may cause serious injury and/or death. Baxter sent a letter to all of its customers, which included advice and instructions to institutions using the infusion pumps.
3-12-09
Read the MedWatch 2009 safety summary, including a link to the Recall Notice, at:
http://www.fda.gov/medwatch/safety/2009/safety09.htm#Colleague
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The Welch Allyn AED 10 Automatic External Defibrillator and MRL JumpStart AED have been recalled due to the possibility of unexpected shutdown, preventing defibrillation of a patient. FDA 3-16-09
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Bodee LLC and FDA notified consumers and healthcare professionals of a nationwide recall of all the company's supplement product sold under the name Zencore Plus. FDA lab analysis of Zencore Plus samples found the product contains benzamidenafil, an undeclared drug product and a PDE5 inhibitor. The use of Zencore Plus by an unsuspecting user of organic nitrates may pose a life-threatening risk of sudden and profound drop of blood pressure due to potential interaction between benzamidenafil and organic nitrates. Zencore Plus is sold in health food stores and by mail order on internet nationwide. Consumers who have this product in their possession should stop using it immediately.
Read the MedWatch safety summary, including a link to the company's Press Release, at:
http://www.fda.gov/medwatch/safety/2009/safety09.htm#Zencore
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