DrugNov 13, 2019
Basic Reset CBD Reset 750 True Full Spectrum Natural Flavor 750 mg CBD 1 fl. oz. (30 mL) recall — FDA D-0193-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
Monthly breakdown
2019 recalls by month
Select a month to review the recall records reported during that period.
December 2019321 records · 4 categoriesNovember 2019597 records · 4 categoriesOctober 2019525 records · 4 categoriesSeptember 2019268 records · 4 categoriesAugust 2019505 records · 4 categoriesJuly 2019680 records · 4 categoriesJune 2019445 records · 4 categoriesMay 2019396 records · 4 categoriesApril 2019242 records · 4 categoriesMarch 2019250 records · 4 categoriesFebruary 2019381 records · 4 categoriesJanuary 2019142 records · 4 categories
2019 recalls — page 36
Records are ordered by the best available source date.
DrugNov 13, 2019
Basic Reset Earth Wash Cleaner and Personal Care, Eco Friendly, Non Toxic, 2 fl.oz. bottle recall — FDA D-0187-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Basic Reset Nuovi Skin Toner, Refined Ionyte, 4 FL recall — FDA D-0189-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets 75 mg, a.) 30 count bottles (NDC 63868-482-30) recall — FDA D-0175-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Sankaijo BOTANICAL LAXATIVE recall — FDA D-0303-2020
Subpotent Drug: Formulated amount of sennosides component is less than labelled claim.
Class IIIFDA: TerminatedSato Pharmaceutical Inc.
DrugNov 13, 2019
Basic Reset CBD Reset 750 True Full Spectrum Cinnamon, 750 mg CBD, 1 fl. oz. (30 mL) bottle recall — FDA D-0192-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Basic Reset Miracle Facelift Masque, All Natural, The Miracle in a Bottle, 2 fl. oz./60 mL recall — FDA D-0188-2020
Marketed without an Approved NDA/ANDA
Class IIFDA: TerminatedBasic Reset Inc.
DrugNov 13, 2019
Dr. Reddy's Laboratories Ranitidine Tablets, USP 150 mg, a.) 65 count bottles recall — FDA D-0171-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
Class IIFDA: CompletedDr. Reddy's Laboratories, Inc.
DrugNov 13, 2019
Green Lumber Natural Fuel For Men capsule recall — FDA D-0351-2020
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain undeclared Tadalafil, an FDA approved drug for the treatment of erectile dysfunction.
Class IFDA: TerminatedGreen Lumber Holdings, LLC
VehicleNov 12, 2019
F-150 cables recall — NHTSA campaign 19V805000
Ford Motor Company (Ford) is recalling certain 2019-2020 F-150 vehicles. The fastener securing the Power Distribution Box (PDB) 12V cable and Battery Monitoring System (BMS) eyelets to the…
cablesFord Motor Company
VehicleNov 8, 2019
Nissan antilock/traction control/electronic limited slip recall — NHTSA campaign 19V807000
Nissan North America, Inc. (Nissan) is recalling certain 2015-2018 Nissan Murano, 2016-2018 Nissan Maxima, and 2017-2019 Nissan Pathfinder and Infiniti QX60 vehicles. These vehicles were…
antilock/traction control/electronic limited slipNissan North America, Inc.
VehicleNov 7, 2019
Palisade side/window recall — NHTSA campaign 19V802000
Hyundai Motor America (Hyundai) is recalling certain 2020 Palisade vehicles. The mounting bolts used to secure the side curtain air bags may damage the side curtain air bags during…
side/windowHyundai Motor America
Medical DeviceNov 6, 2019
OrthoPediatrics Model No. 01-1501-0032 recall — FDA Z-0218-2020
Binding can occur between the attachment bolt and intramedullary nail, which may lead to delays in surgical procedures.
Class IIFDA: TerminatedOrthoPediatrics Corp
Medical DeviceNov 6, 2019
Alto Development A&E Medical Thorecon Plating System Kits Model No. 94-1300-04-S recall — FDA Z-0243-2020
Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes the through-channel for cable tensioning, rendering the tensioner…
Class IIFDA: TerminatedAlto Development Corp
Medical DeviceNov 6, 2019
LivaNova USA SORIN Heater-Cooler System 3T 120V~/60Hz REF 16-02-85 Description of product recall — FDA Z-0220-2020
The firm has become aware that due to a chemical reaction, the disinfectant/water preservative used to disinfect the device to inhibit/limit the growth micro-organisms, may be rendered…
Class IIFDA: TerminatedLivaNova USA Inc.
Medical DeviceNov 6, 2019
Mindray DS USA, Inc. dba Mindray Accutorr 7 Vital Signs Monitor with NIBP valve assembly recall — FDA Z-0236-2020
NIBP valve assembly board subject to this recall includes enhancements that are not included in the current marketing clearance:1. Anti-motion feature 2. NIBP hose blockage identification…
Class IIFDA: TerminatedMindray DS USA, Inc. dba Mindray North America
Medical DeviceNov 6, 2019
Draegar Medical Systems The Infinity Acute Care System (IACS) Monitoring Solution with the recall — FDA Z-0258-2020
Cybersecurity vulnerabilities may cause device to reboot, lose alarm functionality, and/or lose communication with cockpit and/or the Infinity Network.
Class IIFDA: OngoingDraegar Medical Systems, Inc.
Medical DeviceNov 6, 2019
Stryker Neurovascular Synchro2, 0.014in x 200cm, SOFT PRE-SHAPED Guidewire with Hydrophilic recall — FDA Z-0226-2020
The product labels (pouch and carton) for products contain an incorrect value in millimeters (0.036mm) for the Guidewire Outer Diameter dimension. The inches dimension (0.014in) on the…
Class IIFDA: TerminatedStryker Neurovascular
Medical DeviceNov 6, 2019
CRHF Programmers & Remote Monitoring Software Apps: 2090 CareLink Programmer recall — FDA Z-0239-2020
There is a potential for Medtronic programmer and remote monitoring software applications to display an inaccurate remaining longevity estimate for a subset of implanted cardiac device…
Class IIFDA: OngoingMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceNov 6, 2019
Stryker Neurovascular Synchro2, 0.014in x 300cm SOFT Guidewire with Hydrophilic Coating recall — FDA Z-0227-2020
Synchro2, 0.014in x 300cm SOFT Guidewire with Hydrophilic Coating , UPN Product No. M00326310, REF 2631, STERILE:EO - Product Usage: product is intended for general intravascular use,…
Class IIFDA: TerminatedStryker Neurovascular
Medical DeviceNov 6, 2019
Thoratec Switzerland GMBH CentriMag Acute Circulatory Support System Motor, U.S recall — FDA Z-0221-2020
Reports have been received of the CentriMag Systems experiencing motor and pump issues resulting from electromagnetic interference (EMI).
Class IFDA: TerminatedThoratec Switzerland GMBH
Medical DeviceNov 6, 2019
Alto Development A&E Medical Thorecon Plating System Kits Model No. 94-1500-04-S recall — FDA Z-0245-2020
Some Thorecon disposable tensioners supplied in different Plating System Kits exhibit a molding defect which occludes the through-channel for cable tensioning, rendering the tensioner…
Class IIFDA: TerminatedAlto Development Corp
Medical DeviceNov 6, 2019
GE Healthcare CardioLab/ComboLab Recording Systems recall — FDA Z-0257-2020
Potential for failure of the patient leakage current test. There is a potential that if another device with electrical connectivity (e.g., ablation device, ECG monitor) fails, then the CLab…
Class IIFDA: TerminatedGE Healthcare, LLC
Medical DeviceNov 6, 2019
Hycor Biomedical HYTEC Stop Solution (Allergy), 300ml bottle containing 1N sodium hydroxide recall — FDA Z-0224-2020
Some of the Stop Solution bottles, a caustic solution, have been reported to leak.
Class IIFDA: OngoingHycor Biomedical LLC
About the 2019 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.