DrugFeb 8, 2023
Frenda Global Care 70% Alcohol Ethyl Rubbing Alcohol recall — FDA D-0260-2023
cGMP Deviations
Class IIFDA: TerminatedFrenda Corporation
Monthly breakdown
2023 recalls by month
Select a month to review the recall records reported during that period.
December 2023295 records · 4 categoriesNovember 2023387 records · 4 categoriesOctober 2023214 records · 4 categoriesSeptember 2023253 records · 4 categoriesAugust 2023478 records · 4 categoriesJuly 2023263 records · 4 categoriesJune 2023339 records · 4 categoriesMay 2023410 records · 4 categoriesApril 2023189 records · 4 categoriesMarch 2023788 records · 4 categoriesFebruary 2023253 records · 4 categoriesJanuary 2023205 records · 4 categories
2023 recalls — page 160
Records are ordered by the best available source date.
VehicleFeb 2, 2023
General Motors driveshaft recall — NHTSA campaign 23V043000
General Motors, LLC (GM) is recalling certain 2023 Cadillac XT5 and GMC Acadia vehicles. The right-front half-shaft assemblies may be improperly connected to the transmission, causing them…
driveshaftGeneral Motors, LLC
VehicleFeb 2, 2023
General Motors driveshaft recall — NHTSA campaign 23V042000
General Motors, LLC (GM) is recalling certain 2023 Chevrolet Blazer and Traverse vehicles. The left-side half-shaft assemblies may be missing a retaining ring.
driveshaftGeneral Motors, LLC
VehicleFeb 2, 2023
Honda display function recall — NHTSA campaign 23V046000
Honda (American Honda Motor Co.) is recalling certain 2018-2020 Fit and 2019-2022 HR-V vehicles. The rearview camera image may not display when the engine is started with a key, due to a…
display functionHonda (American Honda Motor Co.)
Medical DeviceFeb 1, 2023
TELEFLEX Endotracheal Tube labeled as the following: a recall — FDA Z-1012-2023
Potential for pilot balloon non-inflation or cuff non-deflation.
Class IIFDA: OngoingTELEFLEX LLC
Medical DeviceFeb 1, 2023
SunMed Holdings AirQ3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Size REF recall — FDA Z-1020-2023
There is an orogastric (OG) tube size discrepancy between the labeling in the IFU and the printed text on the device. If the clinician is unable to pass a gastric catheter through one of…
Class IIFDA: OngoingSunMed Holdings, LLC
Medical DeviceFeb 1, 2023
Agfa HealthCare Enterprise Imaging XERO Viewer recall — FDA Z-1004-2023
There is a software defect that can cause issues with images.
Class IIFDA: OngoingAgfa Healthcare NV
Medical DeviceFeb 1, 2023
Johnson & Johnson Surgical Vision Single-Use Packs, REF: OPO80 recall — FDA Z-1007-2023
Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the…
Class IIFDA: OngoingJohnson & Johnson Surgical Vision, Inc.
Medical DeviceFeb 1, 2023
Johnson & Johnson Surgical Vision Veritas Advanced Infusion Packs, REF: VRT-AI recall — FDA Z-1005-2023
Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the…
Class IIFDA: OngoingJohnson & Johnson Surgical Vision, Inc.
Medical DeviceFeb 1, 2023
Abbott Molecular Alinity m System. The Alinity m System is designed to automate the steps recall — FDA Z-1009-2023
The firm identified the following three potential issues which may have impacted ADUs installed on distributed Alinity m Systems. 1. Systems which had their ADUs serviced may have an…
Class IIFDA: OngoingAbbott Molecular, Inc.
Medical DeviceFeb 1, 2023
CooperVision MyDay Toric (90-pack) Reveal 1 Day Toric (90-pack) Soft (hydrophilic) Contact recall — FDA Z-1014-2023
Lenses may be of the incorrect power. A patient who uses an affected lens may experience poor visual acuity.
Class IIFDA: OngoingCooperVision, Inc.
Medical DeviceFeb 1, 2023
Align Technology Invisalign Express 10 REF 8512 Invisalign System Comprehensive REF 9000 recall — FDA Z-1017-2023
3D orthodontic planning software has a defect that leads to an issue where incorrect number of aligners may be produced (less or greater than the doctor requested) and incorrect packaging…
Class IIFDA: CompletedAlign Technology Inc.
Medical DeviceFeb 1, 2023
TELEFLEX Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal recall — FDA Z-1010-2023
Potential for pilot balloon non-inflation or cuff non-deflation.
Class IIFDA: OngoingTELEFLEX LLC
Medical DeviceFeb 1, 2023
Siemens Medical Solutions USA Software : myNeedle Guide 2D license, myNeedle Guide 2D AWP recall — FDA Z-1003-2023
In the syngo.CT VA40 and syngo.CT VA50 myNeedle Guide application, the order of the orientation labels head , center, and feet in the axial thick slice segments are erroneously swapped
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceFeb 1, 2023
Future Diagnostics STAT-IntraOperative-Intact-PTH (STAT-IO-I-PTH) Immunoassay kit REF recall — FDA Z-1016-2023
Due to an issue of high coefficient of variability (CV) problem caused by the accuspheres inside the Immunoassay kits.
Class IIFDA: OngoingFuture Diagnostics Solutions B.V.
Medical DeviceFeb 1, 2023
Biomet Oxford Partial Knee System, Fixed Lateral Tibial Construct- Intended to replace part recall — FDA Z-1018-2023
Packaged in the incorrect shelf carton. Incorrect shelf carton; outer carton is smaller than the required outer carton, which forces the Tyvex pouch to be folded and packaged in the carton…
Class IIFDA: OngoingBiomet, Inc.
Medical DeviceFeb 1, 2023
Getinge Flow-i Anesthesia Systems Flow-i C20, Part no. 6677200 Flow-i C30, Part no. 6677300 recall — FDA Z-0959-2023
Due to a software bug, under certain conditions, pressure cannot be built up resulting in no ventilation. If gas delivery is stopped, a sustained decrease in delivered O2 concentration may…
Class IFDA: OngoingGetinge Usa Sales Inc.
Medical DeviceFeb 1, 2023
Getinge Flow-c Anesthesia System, Part No. 6887700 recall — FDA Z-0960-2023
Due to a software bug, under certain conditions, pressure cannot be built up resulting in no ventilation. If gas delivery is stopped, a sustained decrease in delivered O2 concentration may…
Class IFDA: OngoingGetinge Usa Sales Inc.
Medical DeviceFeb 1, 2023
Johnson & Johnson Surgical Vision FUSION Dual Pump Packs, REF: OPO73 recall — FDA Z-1006-2023
Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the…
Class IIFDA: OngoingJohnson & Johnson Surgical Vision, Inc.
Medical DeviceFeb 1, 2023
Getinge Flow-e Anesthesia System, Part No. 6887900 recall — FDA Z-0961-2023
Due to a software bug, under certain conditions, pressure cannot be built up resulting in no ventilation. If gas delivery is stopped, a sustained decrease in delivered O2 concentration may…
Class IFDA: OngoingGetinge Usa Sales Inc.
Medical DeviceFeb 1, 2023
TELEFLEX Endotracheal Tube labeled as the following: a recall — FDA Z-1011-2023
Potential for pilot balloon non-inflation or cuff non-deflation.
Class IIFDA: OngoingTELEFLEX LLC
Medical DeviceFeb 1, 2023
Meridian Bioscience Revogene SARS-CoV-2_IVD real-time RT-PCR test intended for the recall — FDA Z-1008-2023
Leakage of the original specimen from the plastic microfluidic cartridge (PIE), possibility that laboratory personnel may be exposed to aerosolized specimen containing SARS-CoV-2
Class IIFDA: OngoingMeridian Bioscience Inc.
Medical DeviceFeb 1, 2023
SunMed Holdings Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Size REF Number recall — FDA Z-1019-2023
There is an orogastric (OG) tube size discrepancy between the labeling in the IFU and the printed text on the device. If the clinician is unable to pass a gastric catheter through one of…
Class IIFDA: OngoingSunMed Holdings, LLC
FoodFeb 1, 2023
BAKERY ON MAIN Full Circle Market Organic Oat & Honey Granola recall — FDA F-0315-2023
Product may contain undeclared almonds.
Class IIFDA: TerminatedBAKERY ON MAIN
About the 2023 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.