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, 5:41 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.
781 recalls for “AI”
Medicines & devicesClass II
Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient anesthesia and may lead to intraoperativ
· FDA · Nationwide
FoodClass II
Potential for spoilage.
· FDA · 28 states
FoodClass IIUpdated
Potential foreign material (glass)
· FDA · 19 states
Medicines & devicesClass II
A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift or imprecise control while driving the wheelchair. The wheel
· FDA · Nationwide
Medicines & devicesClass II
Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case condition, rail mechanism may become lodged during operation and moveme
· FDA · Nationwide
FoodClass IIUpdated
Potential contamination with plastic material
· FDA · 41 states
FoodClass IIUpdated
Dietary supplement product Ocular Plus contains undeclared Yellow#5. Dietary supplement product Vista MAX contains undeclared Yellow#5.
· FDA
FoodClass II
Low - Class II · Class II
· USDA FSIS · MN, ND, SD
FoodClass III
Nitrofurans detected in product
· FDA · LA
Medicines & devicesClass II
Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large Esophageal and Tracheal Flange contains a Large Esophageal Flange.
· FDA · Nationwide
Medicines & devicesClass I
Spinal cord stimulation system lead body may be exposed to stress at the anchor site. This may result in high impedance measurements or lead fractures, which may lead to inadequate stimulation, additional intervention, i
· FDA · NY
Medicines & devicesClass II
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to supplier
· FDA · Nationwide
Medicines & devicesClass II
Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit for devices that come into contact with cerebrospina
· FDA · Nationwide
Medicines & devicesClass II
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.
· FDA · Nationwide
Medicines & devicesClass II
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts will not be triggered during the nighttime. This coul
· FDA · Nationwide
Medicines & devicesClass II
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
· FDA · Nationwide
Medicines & devicesClass II
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control
· FDA · Nationwide
Medicines & devicesClass II
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control
· FDA · Nationwide
FoodClass I
Undeclared peanuts.
· FDA · CA
Medicines & devicesClass II
Devices could potentially be occluded or partially occluded.
· FDA · Nationwide
Medicines & devicesClass II
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26 months. The use of a medical device beyond its validated shelf life may resu
· FDA · Nationwide
Medicines & devicesClass II
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the s
· FDA · Nationwide
Medicines & devicesClass II
The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could cause falsely elevated or falsely low total testosterone resul
· FDA · Nationwide
Medicines & devicesClass II
Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification.
· FDA · Nationwide
Medicines & devicesClass II
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
· FDA · Nationwide
Medicines & devicesClass II
Due to a defective circuit board that overheats
· FDA · Nationwide
Medicines & devicesClass II
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator insertion orientation during device preparation. Valve d
· FDA · Nationwide
Medicines & devicesClass II
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.
· FDA
Medicines & devicesClass II
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.
· FDA · 10 states
Medicines & devicesClass I
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or
· 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.