FoodDec 20, 2023
Wilcox Premium Vanilla recall — FDA F-0508-2024
Products may be contaminated with Listeria monocytogenes.
Class IFDA: CompletedWILCOX ICE CREAM
Latest records
Latest recalls — page 469
The newest recall records with useful source details are listed here.
FoodDec 20, 2023
E.A. Sween Co Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units recall — FDA F-0602-2024
Label mix-up and therefore required label information is inaccurate
Class IIIFDA: TerminatedE.A. Sween Co.
FoodDec 20, 2023
Wilcox Premium Maple Cream recall — FDA F-0512-2024
Products may be contaminated with Listeria monocytogenes.
Class IFDA: CompletedWILCOX ICE CREAM
FoodDec 20, 2023
Cut Fruit Express Cut cantaloupe identified with the following Item ID and recall — FDA F-0582-2024
Cantaloupe containing products may be contaminated with Salmonella.
Class IFDA: TerminatedCut Fruit Express, Inc.
FoodDec 20, 2023
Houdini Acorn Raspberry Creme Filled Cookie found in gift basket: #359 recall — FDA F-0593-2024
Undeclared allergens; tree nuts
Class IFDA: TerminatedHoudini Inc.
FoodDec 20, 2023
LGNDS TYSON 2.0, TYSON TONIC KAVA & KRATOM BLEND, FRUIT PUNCH, 2oz recall — FDA F-0505-2024
Finished product contains kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30.
Class IIFDA: TerminatedLGNDS LLC
FoodDec 20, 2023
Cut Fruit Express Mixed Fruit Products that contain Cantaloupe, Honeydew recall — FDA F-0583-2024
Cantaloupe containing products may be contaminated with Salmonella.
Class IFDA: TerminatedCut Fruit Express, Inc.
FoodDec 20, 2023
Houdini Acorn Raspberry Creme Filled Cookie found in gift basket: #197 recall — FDA F-0590-2024
Undeclared allergens; tree nuts
Class IFDA: TerminatedHoudini Inc.
VehicleDec 20, 2023
Volkswagen Group of side/window recall — NHTSA campaign 23V868000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2023-2024 SQ8, RSQ8, Q8, Q7, and 2024 SQ7 vehicles. The driver's seat side air bag may have been improperly mounted to the…
side/windowVolkswagen Group of America, Inc.
DrugDec 20, 2023
Liothyronine Sodium Tablets, USP 5 mcg, 100-count bottle recall — FDA D-0150-2024
Failed Impurities/Degradation Specifications
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
VehicleDec 20, 2023
Toyota Motor Engineering & Manufacturing occupant classification recall — NHTSA campaign 23V865000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2020-2021 Avalon, Avalon Hybrid, Corolla, Highlander, Highlander Hybrid, RAV4, RAV4 Hybrid, Lexus ES350, Lexus RX350,…
occupant classificationToyota Motor Engineering & Manufacturing
VehicleDec 19, 2023
Tesla latch recall — NHTSA campaign 23V862000
Tesla, Inc. (Tesla) is recalling certain 2021-2023 Model S and X vehicles. The cabin doors can be unlocked during a crash. As such, these vehicles fail to comply with the requirements of…
latchTesla, Inc.
VehicleDec 18, 2023
Honda fuel pump recall — NHTSA campaign 23V858000
Honda (American Honda Motor Co.) is recalling certain 2013-2023 Honda Accord, Civic Coupe, Civic Sedan, Civic Hatchback, Civic Type R, CR-V, HR-V, Ridgeline, Odyssey, Acura ILX, MDX, MDX…
fuel pumpHonda (American Honda Motor Co.)
VehicleDec 15, 2023
Maverick bulbs recall — NHTSA campaign 23V848000
Ford Motor Company (Ford) is recalling certain 2022-2024 Maverick vehicles. In the event that one of the rear turn signals stops working, the vehicle will not adjust the turn signal flash…
bulbsFord Motor Company
VehicleDec 15, 2023
Ford column recall — NHTSA campaign 23V847000
Ford Motor Company (Ford) is recalling certain 2023 F-150 and Ford SD F250, F350, F450, F550, and F600 vehicles. The steering wheel clock spring may have an insufficient weld, causing a…
columnFord Motor Company
Medical DeviceDec 13, 2023
Staar Surgical Company EVO+VISIAN Implantable Collamer Lens, REF: VTICM5_12.1 recall — FDA Z-0470-2024
Their is a potential that intraocular implant devices may not meet specifications.
Class IIFDA: OngoingStaar Surgical Company
Medical DeviceDec 13, 2023
Stryker Medical Division of Stryker ProCuity bed series, model number 3009, item number recall — FDA Z-0426-2024
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Class IIFDA: OngoingStryker Medical Division of Stryker Corporation
Medical DeviceDec 13, 2023
Integra LifeSciences Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the recall — FDA Z-0499-2024
Defect in the outer packaging of the Cranial Access Kits. can cause the packaging to split without any additional forces outside compromising the sterility of the device
Class IIFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceDec 13, 2023
Ortho-Clinical Diagnostics VITROS Chemistry Products ECO2 Slides-For in vitro diagnostic use recall — FDA Z-0510-2024
Ortho Clinical Diagnostics (QuidelOrtho) confirmed during routine testing that some lots from Coating 3598 of VITROS ECO2 slides included carts which may contain consecutive slides that may…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceDec 13, 2023
Wilson-Cook Medical QUANTUM TTC BILIARY BALLOON DILATOR, REF QBD-6X3-E, Order Number G22765 recall — FDA Z-0461-2024
Nonconforming devices while manufactured correctly, do not comply to their design requirements. Potential harms associated with balloon detachment are endoscopic retrieval of an impacted or…
Class IIFDA: OngoingWilson-Cook Medical Inc.
Medical DeviceDec 13, 2023
Luminex VERIGENE BC-GP Utility Tray (5-Pack Carrier), Gram-Positive Blood Culture Nucleic recall — FDA Z-0500-2024
Potentially defective utility trays in the reagent kits.
Class IIFDA: OngoingLuminex Corporation
Medical DeviceDec 13, 2023
Stryker Medical Division of Stryker ProCuity bed series, model number 3009, item number recall — FDA Z-0424-2024
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Class IIFDA: OngoingStryker Medical Division of Stryker Corporation
Medical DeviceDec 13, 2023
Stryker Medical Division of Stryker ProCuity bed series, model number 3009, item number recall — FDA Z-0433-2024
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Class IIFDA: OngoingStryker Medical Division of Stryker Corporation
Medical DeviceDec 13, 2023
vyaire Flexible Patient Circuit, 3100A, REF 29028-003, intended to be used with the 3100A recall — FDA Z-0488-2024
Two patient circuits, 29028-003 and 29028-004, for the 3100 High Frequency Oscillatory ventilator that are only approved for use outside the U.S. were distributed in the U.S.
Class IIFDA: CompletedVyaire Medical
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Recent recall archives
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