DrugOct 27, 2021
Imipramine Pamoate Capsules 125 mg, 30-count bottle recall — FDA D-0027-2022
Out of specification result observed in a dissolution test at the 9-month long term stability time point.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
Latest records
Latest recalls — page 808
The newest recall records with useful source details are listed here.
VehicleOct 27, 2021
Palisade fluid recall — NHTSA campaign 21V840000
Hyundai Motor America (Hyundai) is recalling certain 2021 Palisade vehicles. The brake fluid may be contaminated, which can cause the brake master cylinder inner-cup seals to swell, and…
fluidHyundai Motor America
VehicleOct 26, 2021
Rogue Hybrid engine control module (ecu/ecm) recall — NHTSA campaign 21V839000
Nissan North America, Inc. (Nissan) is recalling certain 2017-2019 Rogue Hybrid vehicles. Contact with the Electronic Control Module (ECM) bracket may damage the engine harness, causing a…
engine control module (ecu/ecm)Nissan North America, Inc.
VehicleOct 25, 2021
Tesla curtain recall — NHTSA campaign 21V834000
Tesla, Inc. (Tesla) is recalling certain 2020-2021, 2023 Model 3 vehicles. The left and/or right side curtain air bag may have been improperly secured to the roof rail, which could result…
curtainTesla, Inc.
VehicleOct 25, 2021
Tesla critical fasteners recall — NHTSA campaign 21V835000
Tesla, Inc. (Tesla) is recalling certain 2020-2021 Model Y and 2019-2021 Model 3 vehicles. The front suspension lateral link fasteners may loosen, allowing the lateral link to separate from…
critical fastenersTesla, Inc.
Medical DeviceOct 20, 2021
smiths medical medex HemoDraw Plus Closed Blood Sampling Set with LogiCal Pressure recall — FDA Z-0093-2022
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceOct 20, 2021
Philips recall — FDA Z-0080-2022
Customers were not notified of previous recalls associated with various defibrillator models.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceOct 20, 2021
Bio-Rad Laboratories BioPlex 2200 ANA Screen Control Set, REF: 663-1131 incompatible with recall — FDA Z-0082-2022
A new lot of ANA screen control and any subsequent control lots are incompatible with older lot numbers of ANA calibrators and ANA reagent packs.
Class IIFDA: TerminatedBio-Rad Laboratories, Inc.
Medical DeviceOct 20, 2021
Flower Drill Bit Kit 2.7mm- The Drill Bit Kit, 2.7mm (DBK 027) is intended to be used with recall — FDA Z-0113-2022
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Class IIFDA: TerminatedFlower Orthopedics Corporation
Medical DeviceOct 20, 2021
Philips recall — FDA Z-0078-2022
Customers were not notified of previous recalls associated with various defibrillator models.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceOct 20, 2021
Beckman Coulter Power Processor 3K, 3K High Speed Stockyards Module Nameplate: PP 3K recall — FDA Z-0117-2022
Missing splash guard which may expose users to hazardous materials. .
Class IIFDA: OngoingBeckman Coulter Inc.
Medical DeviceOct 20, 2021
Uoc Usa United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS, 25 recall — FDA Z-0110-2022
Due to product not meeting specification for concentricity and failing to meet requirements of dynamic fatigue testing.
Class IIFDA: TerminatedUoc Usa Inc.
Medical DeviceOct 20, 2021
Abbott Molecular Alinity m Resp-4-Plex AMP Kit recall — FDA Z-0005-2022
There is a potential for false positive results.
Class IFDA: TerminatedAbbott Molecular, Inc.
Medical DeviceOct 20, 2021
Flower Drill Bit Kit 2.4 mm-intended to be used with solid 2.4mm screws and can be used with recall — FDA Z-0112-2022
Drill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
Class IIFDA: TerminatedFlower Orthopedics Corporation
Medical DeviceOct 20, 2021
Draeger Medical Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the recall — FDA Z-0108-2022
Software 2.51 and Lower with Installed CO2 Measurement Option, may result in Restart of the Ventilator, brief cessation of ventilation can occur and loss of PEEP for approx. 8 seconds
Class IIFDA: OngoingDraeger Medical, Inc.
Medical DeviceOct 20, 2021
Inpeco S.A FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) recall — FDA Z-0087-2022
The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur XP/XPT may lead to an incorrect association of test results to sample ID. Improper management of the sample may…
Class IIFDA: OngoingInpeco S.A.
Medical DeviceOct 20, 2021
Philips recall — FDA Z-0079-2022
Customers were not notified of previous recalls associated with various defibrillator models.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceOct 20, 2021
Abbott Molecular Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 recall — FDA Z-0006-2022
There is a potential for false positive results.
Class IFDA: TerminatedAbbott Molecular, Inc.
Medical DeviceOct 20, 2021
National Distribution & Contracting ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel recall — FDA Z-0067-2022
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.
Class IFDA: OngoingNational Distribution & Contracting Inc.
Medical DeviceOct 20, 2021
W L Gore & Associates Heparin, GORE VIABAHN VBX, BALLOON EXPANDABLE ENDOPROTHESIS, REF recall — FDA Z-0077-2022
Incorrect labeling, specifically, expandable endoprosthesis labeled as 8 mm x 59mm x 135 cm, however may contain a 9mm x 29 mm x 135 cm device.
Class IIFDA: OngoingW L Gore & Associates, Inc.
Medical DeviceOct 20, 2021
Red Medical Supplies EcoGel 100 - RED Medical Supplies Green Ultrasound Gel, Model No. recall — FDA Z-0090-2022
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021,FDA published a Letter to Health Care Providers to further…
Class IFDA: OngoingRed Medical Supplies
Medical DeviceOct 20, 2021
Red Medical Supplies EcoGel 200 - RED Medical Supplies Clear Ultrasound Gel, Model No. recall — FDA Z-0089-2022
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021,FDA published a Letter to Health Care Providers to further…
Class IFDA: OngoingRed Medical Supplies
Medical DeviceOct 20, 2021
Abbott Molecular Alinity m SARS-CoV-2 Amp Kit recall — FDA Z-0004-2022
There is a potential for false positive results.
Class IFDA: TerminatedAbbott Molecular, Inc.
Medical DeviceOct 20, 2021
Abbott Molecular Alinity m Resp-4-Plex AMP Kit (Non-US Assay) and Alinity m Resp-4-Plex recall — FDA Z-0008-2022
There is a potential for false positive results.
Class IFDA: TerminatedAbbott Molecular, Inc.
Browse by month
Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 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