FoodPublic Health Alert
FSIS Issues Public Health Alert for Ready-To-Eat Chicken Caesar Wrap Products That May Be Contaminated With Listeria
Public Health Alert · Public Health Alert
· USDA FSIS · MN, WI
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, 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.
1107 recalls
FoodClass I
GELLERT GLOBAL GROUP recalls Fusia
Undeclared Allergen (Fish)
· FDA · CT, MD, NC, NY, PA, TX
Medicines & devicesClass II
Bell Pharmaceuticals, Inc recalls 11 products
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
· FDA · Nationwide
Medicines & devicesClass II
Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeli
Due to incorrect label/product dimensions. Product is supposed to be 3.00 mm in diameter, but unit is packaging was a 2.50 mm in diameter.
· FDA · Nationwide
Medicines & devicesClass II
C.R. Bard Inc recalls 6 products
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
· FDA · Nationwide
Medicines & devicesClass II
Pride Mobility Products Corp. recalls 13 products
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected pa
· FDA · Nationwide
Medicines & devicesClass I
ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ven
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy.
· FDA · Nationwide
FoodClass II
Bear Stewart Co recalls Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough
undeclared soy
· FDA · AZ, CA, NV, UT
FoodClass I
Trafa Pharmaceutical Inc. recalls Trafa Pharmaceuticals Inc
Potential contamination with Salmonella
· FDA · NY
FoodClass I
Lehi Valley Trading Company, Inc recalls High Valley Orchard Chocolate Covered Raisins
Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging.
· FDA · Nationwide
Medicines & devicesClass I
JB Chemicals and Pharmaceuticals Ltd recalls Cetirizine Hydrochloride Tablets USP 5 mg
Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride Tablets USP 5 mg. Determined to be Ranitidine.
· FDA · Nationwide
Medicines & devicesClass II
Reliance Life Sciences Private Limited recalls 4 products
Lack of Sterility Assurance
· FDA · Nationwide
Medicines & devicesClass II
QuVa Pharma, Inc. recalls Methohexital Sodium
Failed Impurities/Degradation Specifications
· FDA · Nationwide
Medicines & devicesClass II
Covidien, LP recalls 5 products
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which may lead to infection, loss of vision if in ophthalmic utilization, or p
· FDA · Nationwide
Medicines & devicesClass II
BioFire Diagnostics, LLC recalls BIOFIRE Respiratory Panel 2
Due to increase in false negative results
· FDA · Nationwide
Medicines & devicesClass II
Maquet Critical Care AB recalls Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30
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
Medicines & devicesClass II
Medtronic Perfusion Systems recalls 6 products
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dys
· FDA · Nationwide
Medicines & devicesClass II
ICU Medical Inc. recalls Hotline Fluid Warming Set
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent application at the tubing to return connector bond.
· FDA · Nationwide
Medicines & devicesClass II
Padagis US LLC recalls Nystatin Cream USP
Subpotent Drug: Low out of specification assay results performed during long-term stability testing.
· FDA · Nationwide
Medicines & devicesClass II
Lupin Pharmaceuticals Inc. recalls Glucagon Emergency Kit for Low Blood Sugar
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
· FDA · Nationwide
Medicines & devicesClass II
Arrowhead DE LLC recalls Arrow-LOK Implant
Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.
· FDA · Nationwide
Medicines & devicesClass II
Therabody, Inc recalls Charger for the Therabody Theragun
Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire). Firm has received reports alleging the product caught fire and other reports regard
· FDA · Nationwide
FoodClass II
AMY'S KITCHEN INC. recalls Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT
Potential for spoilage.
· FDA · 28 states
FoodClass IIUpdated
General Mills James Ford Bell Technical Center recalls 2 products
Potential foreign material (glass)
· FDA · 19 states
FoodClass II
Fayus Inc. recalls OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT
Undeclared peanuts
· FDA · TX
Medicines & devicesClass II
MUNEVO GMBH recalls munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/
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
Ferno-Washington Inc recalls Power F2 Powered Fastening System
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
Medicines & devicesClass II
Boston Scientific Corporation recalls Boston Scientific TheraSphere 360 Y-90 Management Platform
Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more input. When a user modifies an input and selects "Recalculate", the dose ca
· FDA · Nationwide
FoodClass IIUpdated
MARS SNACKING recalls 2 products
Potential contamination with plastic material
· FDA · 41 states
FoodClass IIUpdated
Provision Health Corp. dba PH Labs recalls 2 products
Dietary supplement product Ocular Plus contains undeclared Yellow#5. Dietary supplement product Vista MAX contains undeclared Yellow#5.
· FDA
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.