DrugJul 17, 2024
Verapamil Hydrochloride Injection, USP 10 mg/4 mL (2.5 mg/mL), 5 x 4 mL Single-Dose Vial per recall — FDA D-0593-2024
Cross contamination with other products.
Class IIIFDA: OngoingZydus Pharmaceuticals (USA) Inc.
Latest records
Latest recalls — page 371
The newest recall records with useful source details are listed here.
DrugJul 17, 2024
Verapamil Hydrochloride Injection, USP 5 mg / 2mL(2.5 mg/mL), packaged as (a) 25x2 mL recall — FDA D-0592-2024
Cross contamination with other products.
Class IIIFDA: OngoingZydus Pharmaceuticals (USA) Inc.
VehicleJul 17, 2024
BMW structure recall — NHTSA campaign 24V534000
BMW of North America, LLC (BMW) is recalling certain 2018-2023 X3 sDrive30i, X3 xDrive30i, X3 M40i, and X3 M vehicles. The attachment for the interior cargo rail may become damaged in a…
structureBMW of North America, LLC
VehicleJul 12, 2024
Santa Fe control module software recall — NHTSA campaign 24V529000
Hyundai Motor America (Hyundai) is recalling certain 2024 Santa Fe vehicles. A software error in the transmission control unit may result in a vehicle roll away when the vehicle is in PARK.
control module softwareHyundai Motor America
Medical DeviceJul 10, 2024
MicroPort Orthopedics EVOLUTION MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee recall — FDA Z-2244-2024
One confirmed incident has been received that EFSRN4PR, lot number MP1982170, Size 4 Evolution MP Non-Porous Femoral Right was opened during surgery and contained part number EFSRN3PL, lot…
Class IIFDA: OngoingMicroPort Orthopedics Inc.
Medical DeviceJul 10, 2024
Philips Avalon Ultrasound Transducer recall — FDA Z-2239-2024
Potential for inaccurate fetal heart rate measurements when monitoring multiples.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceJul 10, 2024
GE Medical Systems Information Technologies Prucka 3 Amplifier Model #P1801PA used with recall — FDA Z-2258-2024
Capacitors in certain Prucka 3 Amplifiers used with CardioLab / ComboLab systems could fail resulting in transient oscillations on the display and inability to view surface and intracardiac…
Class IIFDA: OngoingGE Medical Systems Information Technologies Inc.
Medical DeviceJul 10, 2024
First Source iQ Flex M recall — FDA Z-2247-2024
Potential for the bolt that secures the positioning arm to the gas spring to come loose and fall onto patient.
Class IIFDA: OngoingFirst Source Inc.
Medical DeviceJul 10, 2024
MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode recall — FDA Z-2250-2024
To limit the use of the Mega Soft Pads to patients aged 12 or older to mitigate the potential risk of patient burns identified with use of Mega Soft pads.
Class IFDA: OngoingMegadyne Medical Products, Inc.
Medical DeviceJul 10, 2024
MEDLINE INDUSTRIES, LP - Northfield Sterile surgical convenience kit: Medline Retrograde recall — FDA Z-2225-2024
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJul 10, 2024
Siemens AG/Siemens Healthcare GmbH ARTIS is a family of dedicated angiography systems recall — FDA Z-2240-2024
A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release…
Class IIFDA: OngoingSiemens AG/Siemens Healthcare GmbH
Medical DeviceJul 10, 2024
HORIBA custom configured fluorescence instrument, modular Fluorolog-QM recall — FDA Z-2166-2024
HORIBA custom configured fluorescence instrument has a laser safety defect. This custom configuration of the modular Instrument removed the primary light source and the excitation…
Class IIFDA: OngoingHoriba Instruments Inc.
Medical DeviceJul 10, 2024
Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete photometric chemistry recall — FDA Z-2237-2024
The reason for the recall is the pneumatic tubing used in the analytical pick-and-place (PnP) assembly cable may fully or partially disconnect from the flex cable assembly fittings during…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceJul 10, 2024
WOM World Of Medicine AG WOM Tube Set for lrrlgatlon, single-use- Intended to transport recall — FDA Z-2243-2024
Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may result in a delay of surgery
Class IIFDA: OngoingWOM World Of Medicine AG
Medical DeviceJul 10, 2024
Ortho-Clinical Diagnostics VITROS Chemistry Products FS Diluent Pack 3 recall — FDA Z-2266-2024
VITROS Chemistry Products FS Diluent Pack 3, Lot 01-1645 may cause results to be negatively biased when used to dilute patient samples tested with VITROS Chemistry Products CRP Slides.
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 10, 2024
Stryker Curved, super elastic cement delivery needle that passes through the cannula in a recall — FDA Z-2260-2024
Expired Products distributed to customers
Class IIFDA: OngoingStryker Corporation
Medical DeviceJul 10, 2024
Stryker This product is a single use sterile device that is used to direct the lesion to the recall — FDA Z-2261-2024
Expired Products distributed to customers
Class IIFDA: OngoingStryker Corporation
Medical DeviceJul 10, 2024
Zyno Medical Z800, Z800F, Z800W, and Z800WF Infusion Pumps recall — FDA Z-2263-2024
Zyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps have faulty power supply modules that will not provide a charge to the rechargeable battery within the pump. This…
Class IIFDA: OngoingZyno Medical LLC
Medical DeviceJul 10, 2024
MEDLINE INDUSTRIES, LP - Northfield Sterile convenience kit: Medline Birthing Room Pack recall — FDA Z-2227-2024
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJul 10, 2024
MEDLINE INDUSTRIES, LP - Northfield Nonsterile convenience kits: a recall — FDA Z-2229-2024
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJul 10, 2024
Exactech Acumatch L-Series BIPOLAR LINER, 22mm recall — FDA Z-2236-2024
The AcuMatch L-Series 22mm Inner Diameter Bipolar Hip Liner lots were packaged without the specified ethylene vinyl alcohol (EVOH) layer. Between 2004 and August 2021, our packaging process…
Class IIFDA: OngoingExactech, Inc.
Medical DeviceJul 10, 2024
MEGADYNE" MEGA 2000" Patient Return Electrode recall — FDA Z-2248-2024
To limit the use of the Mega Soft Pads to patients aged 12 or older to mitigate the potential risk of patient burns identified with use of Mega Soft pads.
Class IFDA: OngoingMegadyne Medical Products, Inc.
Medical DeviceJul 10, 2024
Olympus Corporation of the Americas EasySuite 4K Integrated Operating Room System recall — FDA Z-2233-2024
A subset of the ES4K systems do not have complete records for earth leakage testing. The earth leakage test is a series of measurements intended to confirm that the amount of electrical…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceJul 10, 2024
MEDLINE INDUSTRIES, LP - Northfield Sterile surgical convenience kits: a recall — FDA Z-2224-2024
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 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 categoriesOctober 2025455 records · 4 categories