Vehicles & car seats
Nissan North America, Inc.: Air Bags May Not Deploy Properly
Air bags that do not deploy as intended increase the risk of injury in a crash.
· NHTSA · Nationwide
Recalls
Safety recalls that rarely make the news, straight from the official U.S. agency records (FDA, USDA, CPSC, NHTSA). Every listing links to its official notice. We only copy what the record says.
Checked Nov 3, 6:23 AM ET · refreshed about every 2.5 hours · RSS · Get recall alerts
State filter: shows recalls whose official distribution lists that state, plus nationwide ones. CPSC and NHTSA recalls apply nationwide.
1107 recalls
FoodClass II
Grand Central Bakery - Oregon Inc. dba Grand Central Bakery, Inc. recalls Product is Potato Sourdough Bread and sold under three following names: Potato Market Loaf 20oz
Foreign object: May contain metal pieces
· FDA · WA
Medicines & devicesClass I
B BRAUN MEDICAL INC recalls Lactated Ringer's Injection USP
Presence of Particulate matter.
· FDA · Nationwide
Medicines & devicesClass II
Medtronic Sofamor Danek USA Inc recalls 2 products
Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to the presence of microbial organisms. While the batch passed
· FDA · Nationwide
Medicines & devicesClass II
Beckman Coulter, Inc. recalls 2 products
The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however, the check valve replacement was excluded from the annual preven
· FDA · Nationwide
Medicines & devicesClass II
BioFire Diagnostics, LLC recalls 3 products
Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results
· FDA · Nationwide
Medicines & devicesClass II
Karl Storz Endoscopy recalls HOPKINS Telescope 30¿
Due to incorrect inside packaging label for eyepiece.
· FDA · Nationwide
Medicines & devicesClass II
INTERVASCULAR, SAS recalls Cardioroot Woven Collagen Coated Vascular Graft
Product failed to meet the specified acceptance criteria for Integral Water Permeability (IWP).
· FDA · Nationwide
Medicines & devicesClass II
CooperVision, Inc. recalls Brand Name: Pearle Vision 1 day Product Name: (somofilcon A) Contact Lens Model/Catalog Number: Pearle Vision
A small number of lenses within the affected lot are of the incorrect power.
· FDA · Nationwide
Medicines & devicesClass I
Abiomed, Inc. recalls 3 products
The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.
· FDA · Nationwide
Medicines & devicesClass II
Straumann USA LLC recalls GM Helix Implant
There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.
· FDA · Nationwide
Vehicles & car seats
Odyne Systems, LLC: High Voltage Battery May Fail and Cause Fire
Battery failure can also increase the risk of a fire.
· NHTSA · Nationwide
Vehicles & car seats
Mack Trucks, Inc.: Marker Lights May Fail to Illuminate/FMVSS 108
Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
Volvo Trucks North America: Marker Lights May Fail to Illuminate/FMVSS 108
Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.
· NHTSA · Nationwide
Vehicles & car seats
BMW of North America, LLC: Loss of Rear Wheel Power from Driveshaft Damage
An unexpected loss of drive power can increase the risk of a crash. In addition, a damaged driveshaft can result in a vehicle rollaway if the parking brake is not applied, increasing the risk of a crash or injury.
· NHTSA · Nationwide
Vehicles & car seats
BMW of North America, LLC: Incorrectly Attached Steering Spindle
An incorrectly attached steering spindle can lead to a loss of steering control, increasing the risk of a crash.
· NHTSA · Nationwide
FoodClass IIUpdated
Byron White Formulas, Inc. recalls 3 products
Label does not declare walnuts in English
· FDA · 50 states
FoodClass II
CUISINE, KETTLE recalls Marketside Tomato Bisque Soup Kit
Product had a presumptive positive test result for Listeria monocytogenes
· FDA · 12 states
Medicines & devicesClass I
American Regent, Inc. recalls Epinephrine Injection
Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and broken and leaking vials.
· FDA · Nationwide
Medicines & devicesClass II
Shanghai United Imaging Healthcare Co., Ltd. recalls 12 products
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from
· FDA · Nationwide
Medicines & devicesKids & BabiesClass I
CooperSurgical, Inc. recalls 2 products
Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure, possibly reducing the effectiveness of treatment and
· FDA · Nationwide
Medicines & devicesClass II
Becton, Dickinson and Company recalls ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oxim
Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.
· FDA · Nationwide
Medicines & devicesClass I
Medline Industries, LP recalls 7 products
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin
· FDA · Nationwide
Medicines & devicesClass II
Baxter Healthcare Corporation recalls 2 products
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.
· FDA · Nationwide
FoodClass II
UPSTATE NIAGARA COOPERATIVE recalls Mehadrin Chocolate Leben
Product may have been improperly pasteurized.
· FDA · NJ
FoodClass II
Africando Foods LLC recalls Clear glass bottle with black screw lid with multi label which reads in part as "***AFRICANDO FOODS
Labeling, wheat not listed as sub ingredient of chicken bouillon (minor ingredient), and soybean oil missing from ingredient list
· FDA · IA, IL, KY
FoodClass I
Lidl US TRADING recalls VITASIA ASIAN STYLE WOK SPICE MIX NET WT 1
Salmonella. The firm received a positive test result of Salmonella in the product.
· FDA · 11 states
Medicines & devicesClass II
Church & Dwight Co., Inc. recalls Zicam
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing
· FDA · Nationwide
Medicines & devicesClass I
Fresenius Kabi USA, LLC recalls Tyenne (tocilizumab-aazg) Injection
Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.
· FDA · Nationwide
Medicines & devicesClass II
AVID Medical, Inc. recalls 15 products
Product may be potentially contaminated with a lubricant used during the manufacturing process.
· FDA · Nationwide
Recall data comes from official U.S. government sources: openFDA (food, drugs, devices), USDA FSIS (meat, poultry, egg products), CPSC (consumer and children’s products) and NHTSA (vehicles, equipment, car seats). openFDA notes its data should not be relied on for medical decisions. Always confirm with the official notice. Check your vehicle by VIN at nhtsa.gov/recalls.