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 · 9 months ago
Olympus Corporation of the Americas Product Name: Single Use 3-Lumen Sphincterotome V recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Single Use 3-Lumen Sphincterotome V recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Etac A/S Brand Name: Molift Product Name: Molift 4-point sling bars Model/ recall: A customer experienced that during assembly and load testing of the device
A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation…
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Class II · 9 months ago
Fujirebio Diagnostics, Inc. Product Name: Lumipulse pTau 217 Plasma Controls Model/ recall: Customers may experience inaccurate test results by observing a higher
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low…
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Disposable Triple Lumen recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Olympus Corporation of the Americas Product Name: Single Use 3-Lumen Sphincterotome V recall: Devices which did not undergo thermoforming could deform and lose performance
Devices which did not undergo thermoforming could deform and lose performance.
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Class II · 9 months ago
Beckman Coulter, Inc. Coulter DxH Diluent, REF 628017 Coulter DxH ECO Diluent REF recall: Due to specific lots of diluents contributing to elevated platelet Daily
Due to specific lots of diluents contributing to elevated platelet Daily Checks background counts cycle with use with analyzers.
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Class II · 9 months ago
Vortex Surgical Inc. Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2 recall: There may be voids located in the seal of Tyvek pouches associated
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has…
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Class II · 9 months ago
Sun Pharmaceutical Industries Inc Diclofenac Sodium, Topical Gel, 3%, 100 g tube recall: Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower
Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.
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Class II · 9 months ago
Granules Pharmaceuticals Inc. Trazodone Hydrochloride, USP, 50 mg, 100-Count Bottle recall: Presence of Foreign Tablets/Capsules
Presence of Foreign Tablets/Capsules
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Class I · 9 months ago
Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10 recall: Marketed without an Approved NDA/ANDA: FDA analysis found this product
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
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Class II · 9 months ago
Unichem Pharmaceuticals USA Inc. Bisoprolol Fumarate and Hydrochlorothiazide tablets recall: cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
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Class III · 9 months ago
Fazt & Loud LLC Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Case recall: Recall is due to a misprint on the label that incorrectly identifies
Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine…
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Class III · 9 months ago
OptiWize Health OptiWize Collagen Plus 320 count bottle recall: The firm initiated a voluntary recall after NSF testing showed that labeled
The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not align with analytical test results…
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Class I · 9 months ago
B.C. Williams Bakery Service, Inc Bread and Roll Mix recall: Undeclared Milk Allergen
Undeclared Milk Allergen
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Class I · 9 months ago
B.C. Williams Bakery Service, Inc Spice Cake Mix recall: Undeclared Milk Allergen
Undeclared Milk Allergen
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Class I · 9 months ago
B.C. Williams Bakery Service, Inc Swiss Chocolate Cake Mix recall: Undeclared Milk Allergen
Undeclared Milk Allergen
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NHTSA safety recall · 9 months ago
Volvo Trucks VNL recall: If the vehicle is in weight bias mode there may not be enough weight
If the vehicle is in weight bias mode there may not be enough weight on the parking brake axle, which could result in inadequate parking brake force.
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NHTSA safety recall · 9 months ago
Hyundai Ioniq 5 and Ioniq 9 recall: The high voltage battery system may contain an improperly tightened bus bar
The high voltage battery system may contain an improperly tightened bus bar, which can cause a short-circuit.
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Highest risk · 9 months ago
Lola Plus The Boys Youth Clothing with Drawstrings recall: Risk of Serious Injury or Death from Strangulation Hazard
Risk of Serious Injury or Death from Strangulation Hazard; Violates Federal Rule for Children's Upper Outerwear
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Highest risk · 9 months ago
Little Cow Company 9 oz Candles in Glass Jars recall: Fire, Burn and Laceration Hazards
Fire, Burn and Laceration Hazards
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Elevated risk · 9 months ago
Clark Associates Lancaster Table & Seating Powder-Coated Aluminum Outdoor Restaurant recall: Fall Hazard
Fall Hazard
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Class II · 9 months ago
CareFusion 303, Inc. BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 recall: Due to a number of modules flashed with a date and time associated
Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue…
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Class II · 9 months ago
Medline medical procedure convenience kits labeled as: Circumcision recall: Medline kits were manufactured and distributed containing MASTISOL liquid
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…