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, 4:38 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
Medicines & devicesClass II
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
· FDA
Medicines & devicesClass II
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
· FDA · Nationwide
Medicines & devicesClass III
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total impurity testing for 12 Month Long-Term Stability.
· FDA · Nationwide
Medicines & devicesClass II
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis machines.
· FDA · Nationwide
Medicines & devicesClass II
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
· FDA · Nationwide
Medicines & devicesClass II
The module did not undergo electrical safety tests and functional tests during production.
· FDA · Nationwide
Medicines & devicesClass II
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life. Reduced bleach concentration may compro
· FDA · Nationwide
Medicines & devicesClass I
Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position.
· FDA · Nationwide
Medicines & devicesClass II
Potential for breach in sterile barrier of device packaging.
· FDA · Nationwide
Medicines & devicesClass II
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
· FDA · Nationwide
Medicines & devicesClass II
The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully discharged into a low-power "shipping mode." When this occurs, an affected d
· FDA · Nationwide
Medicines & devicesClass II
Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the manifold, resulting in loose connection or complete disconnection.
· FDA · Nationwide
Medicines & devicesClass II
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).
· FDA · Nationwide
Medicines & devicesClass II
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries, LP has identified representative samples did not meet applicable perfor
· FDA · Nationwide
Medicines & devicesClass II
Firmware issue potentially leading to loss of geometry movements.
· FDA · Nationwide
Medicines & devicesClass II
Software issue issue with the MAC VU360 v3.0 system. After selecting the order refresh icon, an open preview or review screen might fail to close automatically after 2 minutes of inactivity. As a result, data from a prev
· FDA · Nationwide
Medicines & devicesClass II
Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter, that due to a wire-to-filter-bond issue, may fail to open following sheath retraction; and if this condit
· FDA · Nationwide
FoodClass I
Contaminated with Salmonella
· FDA · Nationwide
Medicines & devicesClass II
Presence of Foreign Tablets/Capsules
· FDA · Nationwide
Medicines & devicesClass II
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
· FDA · Nationwide
Medicines & devicesClass II
Potential of failing to trigger clinical scan during Bolus Tracking.
· FDA · Nationwide
Medicines & devicesClass II
Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits.
· FDA · Nationwide
Medicines & devicesClass II
A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in CO2 leaking into the return path, leading to excessive pressur
· FDA · Nationwide
Medicines & devicesClass III
out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2. While the assay results were not impacted, the overall health risk to lab technicians due to thi
· FDA · Nationwide
Medicines & devicesClass II
Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."
· FDA · Nationwide
Medicines & devicesClass III
Out-of-specification sodium azide concentration in Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1. While the assay results were not impacted, the overall health risk to lab technicians due to this issue is l
· FDA · Nationwide
FoodClass IUpdated
Due to potential E. coli O145:H28 contamination
· FDA · AL, FL, GA, KY, NC, SC, TN, VA
FoodClass IUpdated
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.
· FDA · OR, WA
FoodPublic Health Alert
Public Health Alert · Public Health Alert
· USDA FSIS · 9 states
FoodClass I
High - Class I · Class I
· USDA FSIS · AL, FL, NC, NJ, SC, TN, VA
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.