FoodClass IUpdated
KHONG GUAN (HQ) recalls 2 products
Undeclared peanuts.
· FDA · AZ, CA, CO, HI, NJ, OR, TX, WA
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, 2:58 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
FoodKids & BabiesClass II
PT Organics Limited recalls Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree
Possible foreign object (thin, soft plastic strands).
· FDA · 23 states
Medicines & devicesClass II
Major Pharmaceuticals recalls 12 products
Subpotent Drug
· FDA · Nationwide
Medicines & devicesClass II
Rising Pharma Holding, Inc. recalls Rising
Presence of Precipitate: medication was crystallizing and particles floating in the bottle
· FDA · Nationwide
Medicines & devicesKids & BabiesClass II
Medline Industries, LP recalls 3 products
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localiz
· FDA · Nationwide
Medicines & devicesClass II
Siemens Healthcare Diagnostics, Inc. recalls 2 products
Due to unacceptable precision performance exhibited in certain lots of the Emit 2000 Quinidine Assay, which may lead to erroneously elevated quinidine measurements, creating risk of sub-optimal patient treatment, includi
· FDA · Nationwide
Medicines & devicesClass II
Gentherm Medical, LLC recalls 3 products
Overheating of the 115V CPU board may cause the device to shut down.
· FDA · Nationwide
Medicines & devicesClass II
Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN
Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
· FDA · 20 states
Medicines & devicesClass II
Medtronic MiniMed, Inc. recalls 3 products
Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypog
· FDA
Medicines & devicesClass II
Siemens Healthcare Diagnostics Products Ltd. recalls 2 products
Syphilis Screen assay may contain a negative patient bias resulting in low reactive patient results being reported as nonreactive.
· FDA · Nationwide
Medicines & devicesClass II
Straumann USA LLC recalls GM Helix Implant
There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the incorrect implant is installed, the issue could cause bone compression or dif
· FDA · Nationwide
Medicines & devicesClass II
OBP Medical Corporation recalls OBP Medical
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient and the healthcare provider.
· FDA · Nationwide
FoodClass II
SLT Foods Inc. recalls Khazana The Treasure Spice Magic Fennel Candy
Undeclared Yellow 5 & 6, Red 3, and Blue 1
· FDA · NY
Medicines & devicesClass II
Medline Industries, LP recalls 11 products
Kits contain a potentially contaminated component which were recalled by the manufacturer
· FDA · Nationwide
Medicines & devicesClass II
Medline Industries, LP recalls Medline medical convenience kit labeled as: TRACH TUBE KIT
Component labeling discrepancy
· FDA · Nationwide
Medicines & devicesClass II
AVID Medical, Inc. recalls Halyard LAVH PACK
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
· FDA · Nationwide
Medicines & devicesClass III
Paragon 28, Inc. recalls 2 products
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.
· FDA · Nationwide
Medicines & devicesClass II
GE Medical Systems Information Technologies Inc recalls GE Healthcare Portrait Core Services SW V 1
A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient alarms, and/or access to Protected Health Information (PHI
· FDA · Nationwide
FoodClass II
Pack'n Fresh LLC recalls "***Hondashi 0
Allergen missing from contains statement: fish
· FDA · CA, NJ
Medicines & devicesClass II
CareFusion 213, LLC recalls BD ChloraPrep Clear
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator
· FDA · Nationwide
Medicines & devicesClass III
Medical Action Industries, Inc. 306 recalls Generic Name: Kit
An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027.
· FDA · CA
Medicines & devicesClass II
AVID Medical, Inc. recalls 7 products
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
· FDA · Nationwide
Medicines & devicesClass II
Henry Schein Inc. recalls 2 products
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
· FDA · Nationwide
Medicines & devicesClass I
Boston Scientific Corporation recalls 2 products
Potential for arterial sheath tip separation or partial tip separation during use.
· FDA · Nationwide
Household & products
Best Buy Recalls Insignia® Gas Ranges Due to Risk of Serious Injury from a Fire Hazard
The recalled ranges' front-mounted knobs can be activated accidentally by humans or pets, posing a risk of serious injury from a fire hazard.
· CPSC · Nationwide
Household & products
Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Sold Exclusively on Amazon.com by BBRKIN
The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
· CPSC · Nationwide
Household & products
Conair Recalls Cuisinart Propel+ Four Burner 3-In-1 Gas Grills Due to Risk of Serious Injury from Laceration Hazard
The tempered glass window in the pizza oven can shatter during use, posing a risk of serious injury from laceration hazard.
· CPSC · Nationwide
Household & products
Flaunt Recalls Magsafe Battery Chargers Due to Risk of Serious Injury or Death from Fire and Burn Hazards
The lithium-ion battery in the recalled power banks (chargers) can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards.
· CPSC · Nationwide
Household & products
Greenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batteries Due to Risk of Serious Injury from Fire Hazard
Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit, posing a risk of serious injury from fire hazard.
· CPSC · Nationwide
Household & products
Moodooy Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Yuezhang
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment
· 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.