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, 8:21 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.
781 recalls for “AI”
Medicines & devicesClass II
Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record
· FDA · Nationwide
Medicines & devicesClass II
Due to software malfunction, patient information system may freeze and become unresponsive.
· FDA · Nationwide
Medicines & devicesClass II
The packaging may not consistently maintain sterile barrier integrity.
· FDA · Nationwide
Medicines & devicesClass II
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.
· FDA · Nationwide
FoodPublic Health Alert
Public Health Alert · Public Health Alert
· USDA FSIS · OR, WA
Medicines & devicesClass II
Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling c
· FDA · Nationwide
Medicines & devicesClass II
Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.
· FDA · Nationwide
Medicines & devicesClass II
Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increas
· FDA · Nationwide
Medicines & devicesClass I
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove o
· FDA · 32 states
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
Household & products
The cups and containers violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion haz
· CPSC · Nationwide
Kids & Babies
The recalled dive sticks violate the federal dive sticks ban because they exceeded the compress limit, posing an impalement hazard. In shallow water, children may fall or land on a dive stick, resulting in serious pierci
· CPSC · Nationwide
Kids & Babies
The recalled doll playsets violate the small parts ban because the toys are for children under three years old and some of the accessories are small parts, posing a deadly choking hazard.
· CPSC · Nationwide
Kids & Babies
The zipline kit's steel cable, turnbuckle and seat can detach or break during use, posing a fall hazard. The zipline spring brakes are not stiff enough to safely slow a rider down and the kit design does not include an e
· CPSC · Nationwide
FoodPublic Health Alert
Public Health Alert · Public Health Alert
· USDA FSIS · IL, MI, MN
Medicines & devicesClass II
Failed stability specifications
· FDA · CA
Medicines & devicesClass II
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
· FDA · Nationwide
Medicines & devicesKids & BabiesClass I
A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) bar
· FDA · Nationwide
Medicines & devicesClass II
The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the infusion port during manipulation.
· FDA · Nationwide
Medicines & devicesClass II
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effec
· FDA · Nationwide
Medicines & devicesClass II
Labeling; Oxygen Cylinders do not contain required medical gas labeling
· FDA · Nationwide
FoodClass II
Potential Listeria contamination from dripping condensation in cooler.
· FDA · WI
Medicines & devicesNot Yet Classified
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
· FDA · Nationwide
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 & 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 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
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
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.