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, 12:22 PM 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
Medicines & devicesClass III
Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check.
· FDA · Nationwide
Medicines & devicesClass II
Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fixation or poor alignment of implants, imp
· FDA · Nationwide
Medicines & devicesKids & BabiesClass II
Due to a damaged (over stretched) membrane tail that causes an intermittent fault.
· FDA · Nationwide
FoodClass IIUpdated
Undeclared sulfites Carrot decoration contains Yellow #5 and Yellow #6 which is not listed on finished product label.
· FDA · WI
FoodClass I
High - Class I · Class I
· USDA FSIS · ID, OR, WA
FoodClass II
The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
· FDA · CT, MD, NJ, NY, PA
FoodClass II
Undeclared milk from lactose.
· FDA
Medicines & devicesClass I
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde Presence of Particulate Matter: Product contaminated with particulate matter identified as gl
· FDA · Nationwide
Medicines & devicesClass II
Failed Dissolution Specifications
· FDA · Nationwide
Medicines & devicesClass I
Presence of Particulate Matter
· FDA · Nationwide
Medicines & devicesClass II
Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.
· FDA · Nationwide
Medicines & devicesClass II
Due to a manufacturing issue (inadequate weld) for patient head positioning system.
· FDA · Nationwide
Medicines & devicesClass II
Due to manufacturing issues reperfusion catheters may fracture.
· FDA · Nationwide
Medicines & devicesClass II
The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe, causing a potential risk of false resistant results. False re
· FDA
Medicines & devicesClass II
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
· FDA
FoodClass I
High - Class I · Class I
· USDA FSIS · OK
FoodClass II
Label declares cream and cheese, but Milk is not declared
· FDA · FL
Medicines & devicesClass II
shortfill; reports of empty capsules.
· FDA · Nationwide
Medicines & devicesClass II
CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received.
· FDA · Nationwide
Medicines & devicesClass II
The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a compromised pouch seal is not identified prior
· FDA · Nationwide
Medicines & devicesClass II
Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead
· FDA · Nationwide
Medicines & devicesClass I
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
· FDA · FL, IA, KS, MO, OH, VA
Medicines & devicesClass II
Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.
· FDA · Nationwide
Household & products
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety
· CPSC · Nationwide
Kids & Babies
The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's throat and become lodged, posing a serio
· CPSC · Nationwide
Kids & Babies
The recalled teething toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of a chil
· CPSC · Nationwide
Household & products
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or death to children. The dressers violate the mandatory safety
· CPSC · Nationwide
Household & products
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to consumers.
· CPSC · Nationwide
Kids & Babies
The snap can detach from the recalled bibs and stroller bags, posing a risk of serious injury or death from a choking hazard to young children.
· CPSC · Nationwide
Household & products
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to consumers.
· CPSC · 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.