DrugMar 29, 2023
JARDIANCE (Empagliflozin), 25 mg Tablets recall — FDA D-0468-2023
Labeling: Label Mix-up
Class IIFDA: TerminatedBoehringer Ingelheim Pharmaceuticals, Inc.
March 2023 recalls — page 2
These records include useful source details for the selected month.
VehicleMar 29, 2023
Q7 camera recall — NHTSA campaign 23V212000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2020 Q7 vehicles. Incompatibility between the front camera control software and the heating element used for the front camera…
cameraVolkswagen Group of America, Inc.
VehicleMar 29, 2023
BMW seats recall — NHTSA campaign 23V211000
BMW of North America, LLC (BMW) is recalling certain 2019-2021 330i, 330i xDrive, M340i xDrive, 2020-2021 X3 sDrive30i, X3 xDrive30i, X3 M40i, X3M, 2021 X3 xDrive30e, X4 xDrive30i, and X4M…
seatsBMW of North America, LLC
VehicleMar 29, 2023
Volkswagen Group of front passenger recall — NHTSA campaign 23V215000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2018-2021 Atlas and 2020 Atlas Cross Sport vehicles. The passenger occupant detection system (PODS) may experience a…
front passengerVolkswagen Group of America, Inc.
VehicleMar 24, 2023
Explorer control module (tcm/pcm/tecm) recall — NHTSA campaign 23V199000
Ford Motor Company (Ford) is recalling certain 2020-2022 Explorer vehicles equipped with a 2.3L RWD, 3.3L GAS, 3.3L FHEV, or 3.0L ST powertrain. The previous powertrain control module (PCM)…
control module (tcm/pcm/tecm)Ford Motor Company
VehicleMar 23, 2023
Jeep Wrangler frame and members recall — NHTSA campaign 23V191000
Chrysler (FCA US, LLC) is recalling certain 2020-2022 Jeep Wrangler vehicles. A stud on the frame assembly may puncture the fuel tank in a crash, which can result in a fuel leak.
frame and membersChrysler (FCA US, LLC)
Medical DeviceMar 22, 2023
Synthes (USA) Products TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE recall — FDA Z-1248-2023
TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length, and TFNA Femoral Nails labeled and etched as 170mm may measure 200mm in length
Class IIFDA: OngoingSynthes (USA) Products LLC
Medical DeviceMar 22, 2023
BioFire Diagnostics In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - REF RFIT-ASY-0116 recall — FDA Z-1253-2023
Due to temperature excursions with products (products being stored outside of the required temperature specifications) that may cause a reduction in performance. The temperature excursion…
Class IIFDA: OngoingBioFire Diagnostics, LLC
Medical DeviceMar 22, 2023
Becton Dickinson & Company BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml recall — FDA Z-1238-2023
Nonsterile syringe potentially exposing the patient to pathogenic microorganisms and a risk of local infection.
Class IIFDA: OngoingBecton Dickinson & Company
Medical DeviceMar 22, 2023
Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK recall — FDA Z-1260-2023
The external diameter of the biopsy instrument is larger than the internal diameter of the coaxial needle, which could lead to: 1) Procedural delay, 2) Requirement of an additional device,…
Class IIFDA: OngoingBard Peripheral Vascular Inc.
Medical DeviceMar 22, 2023
BioFire Diagnostics In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1) recall — FDA Z-1252-2023
Due to temperature excursions with products (products being stored outside of the required temperature specifications) that may cause a reduction in performance. The temperature excursion…
Class IIFDA: OngoingBioFire Diagnostics, LLC
Medical DeviceMar 22, 2023
Avanos Medical BALLARD ACCESS Closed Suction System for Neonates/Pediatrics, Y-Manifold recall — FDA Z-1189-2023
Potential for product manifold to crack during use on patients, possibly causing leaks in the respiratory circuit and can lead to the patient receiving inadequate ventilation.
Class IFDA: TerminatedAvanos Medical, Inc.
Medical DeviceMar 22, 2023
Securitas Healthcare Arial mobile application, model #54630 and #54640 for Android devices recall — FDA Z-1250-2023
The mobile application for Android devices downloaded from the Google Play Store do not load per specifications and function on the Android devices.
Class IIFDA: OngoingSecuritas Healthcare LLC
Medical DeviceMar 22, 2023
Avanos Medical BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics, Elbow Manifold recall — FDA Z-1190-2023
Potential for product manifold to crack during use on patients, possibly causing leaks in the respiratory circuit and can lead to the patient receiving inadequate ventilation.
Class IFDA: TerminatedAvanos Medical, Inc.
Medical DeviceMar 22, 2023
Siemens Healthcare Diagnostics Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro recall — FDA Z-1258-2023
Siemens Healthineers has received customer complaints and confirmed imprecision for Quality Control (QC) and patient samples with Dimension Tacrolimus (TAC) lots GA2286, GA3047 and GA3171.…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceMar 22, 2023
Maquet Cardiovascular Fusion Bioline Vascular Graft, Part number M00201503046B0 recall — FDA Z-1245-2023
One (1) Fusion Bioline Vascular graft from lot 25162546, which failed guideline straightness testing, was intermingled with lot 25162549 and distributed to customers. Use of the affected…
Class IIFDA: OngoingMaquet Cardiovascular, LLC
Medical DeviceMar 22, 2023
Beckman Coulter Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N) recall — FDA Z-1257-2023
An increased incidence of damage to the nut band from a new vendor (Boamax) has led to an increased volume of complaints from consignees regarding wash arm motion failures, system check…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceMar 22, 2023
OMM Imports, Inc. dba Zero Gravity Recreo Hair Growth Laser Comb recall — FDA Z-1222-2023
The firm distributed the laser products without affixing the warning, aperture, certification, and identification labels. In addition, the firm failed to provide safety information,…
Class IIFDA: OngoingOMM Imports, Inc. dba Zero Gravity
Medical DeviceMar 22, 2023
Fenwal Amicus MNC Apheresis Kit Double Needle recall — FDA Z-1254-2023
Potential for centrifuge packs to develop a stress leak for certain lots of Amicus MNC Apheresis kit and Amicus Exchange kit (Therapeutic Kits) on the Amicus Separator.
Class IIFDA: OngoingFenwal Inc.
Medical DeviceMar 22, 2023
BioFire Diagnostics In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - REF RFIT-ASY-0147 recall — FDA Z-1251-2023
Due to temperature excursions with products (products being stored outside of the required temperature specifications) that may cause a reduction in performance. The temperature excursion…
Class IIFDA: OngoingBioFire Diagnostics, LLC
Medical DeviceMar 22, 2023
Becton Dickinson & Company BD Ultra-Fine Insulin Syringe 1mL, 6mm, 31G-Insulin Syringes are recall — FDA Z-1241-2023
Nonsterile syringe potentially exposing the patient to pathogenic microorganisms and a risk of local infection.
Class IIFDA: OngoingBecton Dickinson & Company
Medical DeviceMar 22, 2023
Becton Dickinson & Company BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes recall — FDA Z-1243-2023
Nonsterile syringe potentially exposing the patient to pathogenic microorganisms and a risk of local infection.
Class IIFDA: OngoingBecton Dickinson & Company
Medical DeviceMar 22, 2023
Becton Dickinson & Company BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml, 12. recall — FDA Z-1239-2023
Nonsterile syringe potentially exposing the patient to pathogenic microorganisms and a risk of local infection.
Class IIFDA: OngoingBecton Dickinson & Company
Medical DeviceMar 22, 2023
Scientia Vascular Plato 17 Microcatheter: Straight Tip, PL17-160-000 recall — FDA Z-1249-2023
Microcatheters for embolic coil and diagnostic agent introduction to peripheral/neuro vasculature, due to manufacturing non-conformance, and due to flush, guidewire insertion and…
Class IIFDA: OngoingScientia Vascular, Inc.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.