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, 3:52 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
Kids & Babies
The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a fall
· CPSC · Nationwide
FoodClass IIUpdated
Undeclared colors: Yellow#5, and Yellow#6. No labeling. Undeclared wheat and colors: Yellow#5, Yellow#6.
· FDA · CA, NM
FoodClass I
Moringa Powder ingredient positive for salmonella
· FDA
Medicines & devicesClass II
Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications
· FDA · Nationwide
Medicines & devicesClass II
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.
· FDA · Nationwide
Medicines & devicesClass II
Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. This may cause localized heating and gas
· FDA · Nationwide
Medicines & devicesClass II
The Automated Field Steam Sterilizer's water recovery system 120V Amphenol connector may experience an intermittent loss of ground continuity, which could result in an unreliable fault current return path.
· FDA · Nationwide
Medicines & devicesClass II
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
· FDA · Nationwide
Medicines & devicesClass II
Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.
· FDA · Nationwide
FoodClass I
Undeclared milk.
· FDA · CA, GA, IL, NJ, NY, TX
Medicines & devicesClass III
Failed Dissolution Specifications
· FDA · Nationwide
Medicines & devicesClass II
Lack of Assurance of Sterility
· FDA · Nationwide
Medicines & devicesClass II
Transfemoral catheter, positing arm may detached due to weld issue.
· FDA · Nationwide
Medicines & devicesClass II
Urostomy Pouches may leak from cap during use.
· FDA · Nationwide
Medicines & devicesClass I
Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised, patients may be exposed to microorganisms, endotoxins, or foreign matter. This m
· FDA · CA, FL, NC, OK, TX, VA
Medicines & devicesClass II
The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could lead to a prolonged or modified surgery as the plateau cannot be inserted
· FDA · IN
Medicines & devicesClass II
Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely depressed Atellica CH Enzymatic Hemoglobin A1c (A1c_E) results;
· FDA · Nationwide
FoodPublic Health Alert
Public Health Alert · Public Health Alert
· USDA FSIS · OK
FoodClass I
Potential E. coli O145:H28 Contamination
· FDA · FL
FoodClass II
Staphylococcus aureus detected in product.
· FDA · Nationwide
FoodClass II
Ambient storage of the product may lead to Clostridium botulinum toxin formation.
· FDA · NJ, NY
Medicines & devicesClass II
Presence of precipitate
· FDA · Nationwide
Medicines & devicesClass II
Potential for false negative patient results.
· FDA · Nationwide
Medicines & devicesClass II
Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with approx. 4.5 cc DBM (fill for 45 ¿ 11 mm configuration)
· FDA · Nationwide
FoodClass IIUpdated
Foreign Manufacturer label contains Undeclared allergen ingredients Wheat, Soy, Sesame, Yellow #5 and Blue #1 in Frozen Flounder Products.
· FDA · CA, NJ
FoodClass II
Product label allergen "contains" statement does not include anchovy(fish)
· FDA
FoodClass II
Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
· FDA · Nationwide
Medicines & devicesClass I
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
· FDA · Nationwide
Medicines & devicesClass II
Device will intermittently provide inaccurate data related to native heart rate.
· FDA · Nationwide
Medicines & devicesClass II
Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linea
· 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.