Recalls affecting Vermont
Notices that name Vermont in their distribution area, plus every nationwide recall — nationwide recalls reach Vermont too.
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Class II · 6 months ago
Wells Pharma of Houston LLC Ketamine Hydrochloride Injectable Solution recall: cGMP deviations
cGMP deviations.
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Class II · 6 months ago
Thea Pharma, Inc. Similasan, iVIZIA, Sterile Lubricant Eye Drops , 0.33 Fl oz recall: Lack of Assurance of Sterility: This recall has been initiated due to CGMP
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer.
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Class II · 6 months ago
King Juice Company, Inc. Calypso Tropic Tango Lemonade. 16 FL oz recall: Product contains undeclared Yellow No. 5
Product contains undeclared Yellow No. 5.
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Class II · 6 months ago
The Mochi Ice Cream Company, LLC My Mochi Strawberry flavored Non-Dairy Frozen Dessert recall: Foreign object found inside retail container
Foreign object found inside retail container.
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Elevated risk · 6 months ago
My Wife’s Slaw Original and Jalapeno Heat flavored coleslaw recall: Foodborne Illness - Potential for microorganisms growth
Foodborne Illness - Potential for microorganisms growth
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Class I · 6 months ago
Zapp’s, Dirty Potato chips recall: Potential Foodborne Illness - Salmonella
Potential Foodborne Illness - Salmonella
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Class I · 6 months ago
a2 a2 Platinum Premium Infant Formula 0-12 months USA label recall: Presence of cereulide toxin produced by some strains of the bacterium
Presence of cereulide toxin produced by some strains of the bacterium Bacillus cereus
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Class II · 6 months ago
Second Nature Keto Crunch Smart Mix recall: May contain undeclared Cashews, Pistachios, and Cherries
May contain undeclared Cashews, Pistachios, and Cherries
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NHTSA safety recall · 6 months ago
Mercedes-Benz CLA 350 4MATIC and CLA 250+ recall: The front passenger seat belt retractor may have been manufactured
The front passenger seat belt retractor may have been manufactured with a defect that prevents the deactivation of the child seat safety function…
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NHTSA safety recall · 6 months ago
Mercedes-Benz recall: The infotainment control unit may reset while the vehicle is in motion
The infotainment control unit may reset while the vehicle is in motion and cause the instrument panel display to go blank.
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Highest risk · 6 months ago
Thermos 8.2 Million Stainless King Food Jars and Bottles recall: Serious Impact Injury and Laceration Hazards
Serious Impact Injury and Laceration Hazards
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Highest risk · 6 months ago
Residential Elevators Elevator StrikeLock Hoistway Door Locking Device recall: Risk of Serious Injury or Death from Fall and Injury Hazards
Risk of Serious Injury or Death from Fall and Injury Hazards
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Highest risk · 6 months ago
CBC Group Stephan Baby Boo Bunnie and Friends Children's Toys recall: Risk of Serious Injury from Choking and Laceration Hazards
Risk of Serious Injury from Choking and Laceration Hazards
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Highest risk · 6 months ago
American Honda Motor Off-Road Motorcycles recall: Risk of Serious Injury or Death Due to Crash Hazard
Risk of Serious Injury or Death Due to Crash Hazard
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Public Health Alert · 6 months ago
FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Dairy Products That Have Been Recalled Due to Possible…
Product Contamination
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Class II · 6 months ago
Olympus Corporation of the Americas OER-ELITE Endoscope Reprocessor Connecting Tubes recall: Potential for the Version 2 reprocessor connecting tube lock levers may fail
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
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Class II · 6 months ago
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate recall: Unapproved design changes to the products outside of the 510(k) clearance
Unapproved design changes to the products outside of the 510(k) clearance.
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Class II · 6 months ago
Medline Kits: 1) Arthrogram Tray recall: The 510(k) regulatory clearances for certain Control Syringes
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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Class II · 6 months ago
Medline Kits: 1) D AND C PACK recall: The 510(k) regulatory clearances for certain Control Syringes
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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Class II · 6 months ago
Angiodynamics, Inc. Soft-Vu Angiographic Catheter, Headhunter , Non-Braided recall: The affected devices contain a manufacturing defect which may prevent
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID)…
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Class II · 6 months ago
XTANT Medical Holdings, Inc nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus recall: Products were incorrectly labeled with a 5-year shelf life. The approved
Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.
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Class II · 6 months ago
Angiodynamics, Inc. Soft -Vu Angiographic Catheter, Kumpe, Non-Braided recall: The affected devices contain a manufacturing defect which may prevent
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID)…
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Class II · 6 months ago
Angiodynamics, Inc. Soft-Vu Angiographic Catheter, Cobra , Non-Braided recall: The affected devices contain a manufacturing defect which may prevent
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID)…
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Class II · 6 months ago
Remel Europe Ltd. Oxoid Agglutinating Sera, Salmonella 9-0 R30957301 recall: Affected lots are not performing to IFU criteria showing cross reactions
Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the…