DrugAug 30, 2023
Parker Laboratories Helix CBD Therapy Cream (Menthol 7.4%) recall — FDA D-1092-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
Latest records
Latest recalls — page 513
The newest recall records with useful source details are listed here.
DrugAug 30, 2023
Ecometics Blis-To-Sol Liquid (Tolnaftate), 1% recall — FDA D-1096-2023
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Class IIFDA: CompletedEcometics, Inc.
DrugAug 30, 2023
Parker Laboratories Helix Tri-Active Therapy Cream recall — FDA D-1091-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
DrugAug 30, 2023
Ecometics ALCOLADO RELAMPAGO (Menthol and Camphor), 1% and 1.5% respectively recall — FDA D-1098-2023
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Class IIFDA: CompletedEcometics, Inc.
DrugAug 30, 2023
Ecometics Lugol's recall — FDA D-1102-2023
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Class IIFDA: CompletedEcometics, Inc.
DrugAug 30, 2023
Parker Laboratories Helix Pain Relieving Cream (Menthol 7.4%) recall — FDA D-1090-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
VehicleAug 30, 2023
Volkswagen Group of switch recall — NHTSA campaign 23V604000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Golf, Golf Alltrack, Golf Sportwagen, 2019-2020 Golf GTI, and Jetta vehicles equipped with a conventional ignition…
switchVolkswagen Group of America, Inc.
VehicleAug 25, 2023
Volkswagen Group of fluid recall — NHTSA campaign 23V601000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2021 Audi S7, S6 Sedan, RS7, RS6 Avant, A6 Allroad, 2019-2021 A7, and A6 Sedan vehicles. An incorrectly labeled brake fluid cap…
fluidVolkswagen Group of America, Inc.
VehicleAug 25, 2023
Palisade front passenger recall — NHTSA campaign 23V599000
Hyundai Motor America (Hyundai) is recalling certain 2024 Palisade vehicles equipped with dark premium suede seats. The Occupant Detection System (ODS) may fail to detect an occupant and…
front passengerHyundai Motor America
VehicleAug 25, 2023
Ford camera recall — NHTSA campaign 23V598000
Ford Motor Company (Ford) is recalling certain 2020-2023 Lincoln Aviator, 2018-2021 Lincoln Navigator, 2022-2023 Ford Transit, and 2021 Ford Bronco vehicles. The rearview camera, or…
cameraFord Motor Company
VehicleAug 25, 2023
Explorer turbo/supercharger recall — NHTSA campaign 23V597000
Ford Motor Company (Ford) is recalling certain 2023 Explorer vehicles equipped with 2.3L GTDI engines. The turbocharger oil supply line may be damaged, which can result in an oil leak…
turbo/superchargerFord Motor Company
Medical DeviceAug 23, 2023
Carefusion 2200 Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 45CM, RATCHETED recall — FDA Z-2429-2023
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceAug 23, 2023
Carefusion 2200 Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 45CM recall — FDA Z-2426-2023
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved recall — FDA Z-2389-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight recall — FDA Z-2381-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved recall — FDA Z-2387-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved recall — FDA Z-2367-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved recall — FDA Z-2375-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Carefusion 2200 Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 32CM, RATCHETED recall — FDA Z-2425-2023
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceAug 23, 2023
Carefusion 2200 Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 25 MM JAW 5MM, 32CM recall — FDA Z-2419-2023
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceAug 23, 2023
Carefusion 2200 Snowden-Pencer MIS DIAMOND-TOUCH GRASPERS CROCODILE GRASPER, DOUBLE ACTI recall — FDA Z-2424-2023
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved recall — FDA Z-2370-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved recall — FDA Z-2385-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Alcon Research Phaco Standalone Tips recall — FDA Z-2410-2023
Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.
Class IIFDA: OngoingAlcon Research, LTD.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories