DrugSep 25, 2019
Ridge Properties Soothing Sore Relief (lidocaine) Cream, 4% recall — FDA D-1860-2019
Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.
Class IIFDA: TerminatedRidge Properties, LLC
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 64
Records are ordered by the best available source date.
DrugSep 25, 2019
Ridge Properties Soothing Sore Relief (lidocaine) Liquid Gel, 4% recall — FDA D-1861-2019
Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.
Class IIFDA: TerminatedRidge Properties, LLC
DrugSep 25, 2019
Ridge Properties PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Cream, 4% recall — FDA D-1856-2019
Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.
Class IIFDA: TerminatedRidge Properties, LLC
DrugSep 25, 2019
Anagrelide Capsules, USP, 0.5 mg, 100-count bottle recall — FDA D-1862-2019
Failed Impurities/Degradation Specifications: High Out Of Specification results for impurities detected during routine stability testing.
Class IIFDA: TerminatedTorrent Pharma Inc.
DrugSep 25, 2019
Ridge Properties Superior Pain & Itch Relief (lidocaine) Liquid Gel, 4% recall — FDA D-1859-2019
Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.
Class IIFDA: TerminatedRidge Properties, LLC
DrugSep 25, 2019
Ridge Properties PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Liquid Gel, 4% recall — FDA D-1857-2019
Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.
Class IIFDA: TerminatedRidge Properties, LLC
VehicleSep 25, 2019
BMW front recall — NHTSA campaign 19V678000
BMW of North America, LLC (BMW) is recalling certain 2020 X3 sDrive30i, X3 xDrive30i, and X3 M40i vehicles, X4 xDrive30i, and X4 M40i vehicles. The front axle swivel bearings may not have…
frontBMW of North America, LLC
VehicleSep 25, 2019
Volkswagen Group of unknown or other recall — NHTSA campaign 19V679000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2017 Volkswagen Passat, 2018 Tiguan LWB, 2007-2009 Jetta Sedan, 2011-2013, 2015 and 2019 Jetta, 2013 Jetta Hybrid,…
unknown or otherVolkswagen Group of America, Inc.
VehicleSep 20, 2019
Toyota 4Runner steering recall — NHTSA campaign 19V670000
Southeast Toyota Distributors, LLC (SET) is recalling certain 2018-2019 Toyota 4Runner vehicles. During installation, certain steering and suspension components may not have been properly…
steeringSoutheast Toyota Distributors, LLC
VehicleSep 19, 2019
Chevrolet Equinox all-wheel drive tank recall — NHTSA campaign 19V667000
General Motors LLC (GM) is recalling certain 2019-2020 Chevrolet Equinox all-wheel drive vehicles. The fuel tanks may have been manufactured with an improperly sealed seam, possibly…
tankGeneral Motors LLC
Medical DeviceSep 18, 2019
Allergan PLC RITZ PRINCESS, BIOCELL, INTRASHIEL, BioDIMENSIONAL Breast Implant, Styles RML recall — FDA Z-2464-2019
The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma…
Class IFDA: OngoingAllergan PLC
Medical DeviceSep 18, 2019
CRHF Medtronic Micra MC1VR01, Single chamber transcatheter pacing system, REF MC1VR01US recall — FDA Z-2492-2019
Medtronic is updating the Micra Instructions for Use (IFU) and the Micra Implant Procedure Tip Card to include specific information on the removal of the tether to release the Micra…
Class IIFDA: TerminatedMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Medical DeviceSep 18, 2019
Zeus Scientific Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay File recall — FDA Z-2494-2019
Assay files used on the open Dynex DSX Instrument to process IVD ELISA samples-programming error results in well H6 being skipped for the addition of the TMB substrate. Well H6 will…
Class IIFDA: TerminatedZeus Scientific, Inc.
Medical DeviceSep 18, 2019
Randox Laboratories This is an in vitro diagnostic product intended for use as a calibration recall — FDA Z-2490-2019
Randox Laboratories realigned RX Analyser Series calibration targets by 10% for AST and 9% for ALT in line with the Mean of All Instrument method target for the Randox Calibration Serum…
Class IIIFDA: TerminatedRandox Laboratories Ltd.
Medical DeviceSep 18, 2019
Exactech Threaded Offset Cup Impactor - Product Usage: To assist the surgeon in the recall — FDA Z-2499-2019
The threaded mechanism of the Threaded Offset Cup Impactor may be gritty and difficult to turn potentially due to entrapped blast media.
Class IIFDA: TerminatedExactech, Inc.
Medical DeviceSep 18, 2019
Allergan PLC McGhan BioDIMENSIONAL silicone-Filled Breast Implants, style 153 Product Usage recall — FDA Z-2459-2019
The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma…
Class IFDA: OngoingAllergan PLC
Medical DeviceSep 18, 2019
Allergan PLC Natrelle 510, TruForm, Dual-Gel, BIOCELL, Styles LX, MX, FX Product Usage recall — FDA Z-2461-2019
The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma…
Class IFDA: OngoingAllergan PLC
Medical DeviceSep 18, 2019
Teleflex Medical Sheridan/CF Novaplus 7.0 mm, REF V5-10114 Product Usage: Tracheal recall — FDA Z-2317-2019
Reported complaints indicate an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the endotracheal tube (ETT). Disconnection from the breathing…
Class IFDA: TerminatedTeleflex Medical
Medical DeviceSep 18, 2019
Allergan PLC Natrelle 410, Highly Cohesive Anatomically Shaped Silicone-Filled Breast recall — FDA Z-2452-2019
The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma…
Class IFDA: OngoingAllergan PLC
Medical DeviceSep 18, 2019
Allergan PLC Natrelle 133 Tissue Expanders recall — FDA Z-2455-2019
The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma…
Class IFDA: OngoingAllergan PLC
Medical DeviceSep 18, 2019
Allergan PLC Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable recall — FDA Z-2457-2019
The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma…
Class IFDA: OngoingAllergan PLC
Medical DeviceSep 18, 2019
Allergan PLC Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate recall — FDA Z-2454-2019
The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma…
Class IFDA: OngoingAllergan PLC
Medical DeviceSep 18, 2019
Teleflex Medical Sheridan/HVT Novaplus: a) 7.0 mm, REF V5-10314 b) 7.5 mm, REF V5-10315 c) recall — FDA Z-2318-2019
Reported complaints indicate an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the endotracheal tube (ETT). Disconnection from the breathing…
Class IFDA: TerminatedTeleflex Medical
Medical DeviceSep 18, 2019
Teleflex Medical Hudson RCI Sheridan LTS: a) 4.0 mm, REF 5-11108 b) 5.0 mm, REF 5-11110 c) recall — FDA Z-2311-2019
Reported complaints indicate an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the endotracheal tube (ETT). Disconnection from the breathing…
Class IFDA: TerminatedTeleflex Medical
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.