FoodFeb 26, 2020
CSM Bakery Products 40 lb recall — FDA F-0722-2020
Pieces of plastic polymer were introduced into the sugar system.
Class IIFDA: TerminatedCSM Bakery Products
Latest records
Latest recalls — page 1075
The newest recall records with useful source details are listed here.
FoodFeb 26, 2020
The Honest Stand Hungry Root Dairy free Garlic Parm sauce, Packaged in 9 oz recall — FDA F-0711-2020
Undeclared Allergen: Product contains both cashews and almonds, but only almonds were labeled on the physical product. Both allergens were labeled on the electronic ingredient statement…
Class IFDA: TerminatedThe Honest Stand
FoodFeb 26, 2020
CSM Bakery Products 35 lb recall — FDA F-0728-2020
Pieces of plastic polymer were introduced into the sugar system.
Class IIFDA: TerminatedCSM Bakery Products
FoodFeb 26, 2020
New Seasons Market Vegetarian Lasagna With Gluten-Free Pasta, New Seasons Market recall — FDA F-0713-2020
Undeclared Soy. BBQ sauce was inadvertently used instead of Marinara sauce and BBQ sauce contains soy. The Vegetarian Lasagna finished product label does not declare soy.
Class IIFDA: TerminatedNew Seasons Market LLC
DrugFeb 26, 2020
Memantine Hydrochloride Extended-release Capsules, 28mg recall — FDA D-0844-2020
Failed Dissolution Specifications: High out of specification result observed at stability studies.
Class IIIFDA: TerminatedThe Harvard Drug Group
DrugFeb 26, 2020
Glycopyrrolate Injection, USP 4 mg per 20 mL (0.2 mg/mL), 20 mL Multiple Dose Vial recall — FDA D-0853-2020
Failed Impurities/Degradation Specifications: elevated levels of Benzaldehyde impurity was found in investigative samples (retain samples).
Class IIIFDA: TerminatedAuroMedics Pharma LLC
DrugFeb 26, 2020
Teva Pharmaceuticals USA Tramadol Hydrochloride Tablets USP CIV, 50 mg recall — FDA D-0851-2020
Labeling: Incorrect package insert - Patient leaflets for the specified lots of unscored tablets contain language relative to a 25 mg dosing titration that necessitates the use of a scored…
Class IIIFDA: TerminatedTeva Pharmaceuticals USA
DrugFeb 26, 2020
American Health Packaging Desmopressin Acetate Tablets, 0.2 mg, 30 tablets recall — FDA D-0849-2020
GMP Deviations: Product bottle may be absent of desiccant.
Class IIFDA: TerminatedAmerican Health Packaging
DrugFeb 26, 2020
American Health Packaging Desmopressin Acetate Tablets, 0.1 mg, 30 tablets recall — FDA D-0848-2020
GMP Deviations: Product bottle may be absent of desiccant.
Class IIFDA: TerminatedAmerican Health Packaging
VehicleFeb 21, 2020
Ford headlights recall — NHTSA campaign 20V097000
Ford Motor Company (Ford) is recalling certain 2018-2020 F-150 trucks equipped with high series LED headlamps with Autolamp (On/Off) functionality. The Daytime Running Lamps (DRL) may…
headlightsFord Motor Company
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Kit, Product Code TI-05501-ME recall — FDA Z-1212-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR Peripheral Coil System, Detachable 35, Framing Coil, REF numbers recall — FDA Z-1224-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Kit, Product Code YC-02220 recall — FDA Z-1217-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Philips VesselNavigator application used with Philips Azurion (Azurion 7 Series) Software recall — FDA Z-1145-2020
Due to a software defect, when a digital subtraction angiography (DSA) is exported to the VesselNavigator application, the DSA is displayed without subtraction.
Class IIFDA: TerminatedPhilips North America, LLC
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR CX Peripheral Coil System, Detachable 18, CX Coil, REF numbers recall — FDA Z-1222-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
TELEFLEX MEDICAL HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote recall — FDA Z-1113-2020
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column…
Class IFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceFeb 19, 2020
Respironics V680 Ventilator, Service # 850011, (OUS Only) recall — FDA Z-1155-2020
Ventilator touchscreen may become frozen and fail to respond to touch commands. If a patient requires a change in therapy, there is no warning associated with an unresponsive touchcreen,…
Class IIFDA: OngoingRespironics California, LLC
Medical DeviceFeb 19, 2020
Arrow International EPIDURAL CATHETERIZATION KIT, Product Code MTO-09903-KU recall — FDA Z-1210-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
TELEFLEX MEDICAL HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port recall — FDA Z-1115-2020
There is the potential for water to flood the column and enter the circuit under circumstances where an abnormal pressure differential is created between the water bottle and the column…
Class IFDA: TerminatedTELEFLEX MEDICAL Inc.
Medical DeviceFeb 19, 2020
Microvention Terumo AZUR Peripheral Coil System, Detachable 35, Helical HydroCoil recall — FDA Z-1223-2020
The devices may be missing the implant coil.
Class IIFDA: TerminatedMicrovention, Inc.
Medical DeviceFeb 19, 2020
Taewoong Medical Co Niti-S Esophageal Stent, REF ES1806F, ES1808F, ES1810F, ES1815F recall — FDA Z-1229-2020
Misprinted IFUs shipped with esophageal stents
Class IIFDA: TerminatedTaewoong Medical Co., Ltd.
Medical DeviceFeb 19, 2020
Arrow International FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05503-BID recall — FDA Z-1182-2020
There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
Class IIFDA: TerminatedArrow International Inc.
Medical DeviceFeb 19, 2020
Pacific Medical Group Ultrasound Transducer (M2736A), that may have been serviced with the recall — FDA Z-1167-2020
Fetal/maternal monitor/monitoring systems serviced or remanufactured using non-OEM equivalent components that have not been appropriately verified or validated. Possible adverse clinical…
Class IIFDA: OngoingPacific Medical Group Inc.
Medical DeviceFeb 19, 2020
Flowonix Medical Prometra II 40mL Pump recall — FDA Z-1122-2020
A pump alarm function anomaly in the pump firmware code may result in the pump not sending the expected error code notifications to the Programmer, or not emit an audible alarm tone in…
Class IIFDA: OngoingFlowonix Medical Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026180 records · 4 categoriesSeptember 2026363 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 categories