Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,836 recalls, newest first · Checked 10 minutes ago
United StatesBecton Dickinson & Co. recalls BD Phoenix Panel NMIC-312. Catalog Number: 449082. and 1 more products
Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.Sarnova HC, Llc recalls Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack
Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.Integrated Medcraft LLC recalls FORWARD Gunshot Wound Kit
Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the sterile pad…Ethicon, LLC recalls PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture
Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that if…W L Gore & Associates, Inc. recalls Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis
The potential for the devices to be mislabeled with the incorrect length.Microgenics Corporation recalls MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control
Vial-to-vial variability in MAS¿ Omni"IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone (PTH)…Steris Corporation recalls RAPICIDE PA Part A High-Level Disinfectant and 2 more products
If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure.Jenavalve Technology Inc. recalls JenaValve Trilogy Delivery Catheter and 2 more products
Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device.In2bones USA, LLC recalls REF: P65 ST862 CoLag SCREW
Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws.SI-BONE, Inc. recalls iFuse TORQ Implant System Model/Catalog Number: 10055T
The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured.Cadwell Industries Inc recalls Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number: 190296-200…
Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the patient…Radiometer Medical ApS recalls The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists
In vitro diagnostic analyzer had a risk of potentially inaccurate results requiring changes to instructions for use and: 1) Sample types, including whole blood samples…Intelerad Medical Systems Incorporated recalls IntelePACS
Following a Chromium-based web-browser, report and displayed images may not match.BioFire Diagnostics, LLC recalls Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel… and 2 more products
Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive resultsBeckman Coulter, Inc. recalls DxU 840m Iris and 1 more products
The rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage; however, the check…Baxter Healthcare Corporation recalls Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product…
Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap…Magellan Diagnostics, Inc. recalls LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762.
In kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the correct expiration date…Medline Industries, LP recalls Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135… and 5 more products
Kits contain CONMED AirSeal Access Ports.Medline Industries, LP recalls Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A
Discrepancy in the shelf-life of a componentMedtronic Sofamor Danek USA Inc recalls Grafton" DBM and Grafton Plus" DBM contain demineralized human bone tissue combined with…
Medtronic identified through donor record review that the donor for Medtronic batch A62881 did not meet all Medtronic donor eligibility requirements related to the…Cook Incorporated recalls Williams Cystoscopic Injection Needles
The female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing during manufacturing.Instrumentation Laboratory recalls HemoslL AcuStar HIT-lgG and 1 more products
Potential for invalid calibration curve or negative mean bias of up to 47% with patient samples.Medline Industries, LP recalls Medline surgical convenience kits labeled as: CABG AUXILIARY PACK and 11 more products
Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or…A little guidance
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