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.
3,853 recalls, newest first · Checked 8 minutes ago
United StatesBendix EC80 Advanced Electronic Control Units (ECU) part numbers K219877SC001 and other models recall: ECU malfunction may impair safety systems
Safety systems that depend on the ECU (Automatic Traction Control, ABS, Electronic Stability Control, Active Cruise Control, and Collison Mitigation System) may have…2020-2026 Western Star 49X and other models recall: Loss of vehicle control from loose axle clamp fasteners
A loss of vehicle control increases the risk of a crash.2024-2026 Shuttle transit buses equipped with wheel chair restraint retractors recall: Wheelchair restraint retractor may not lock
An unlocked wheelchair can move during transit or during a crash, increasing the risk of injury.one Tuftrac Gen 2 suspension assembly recall: Loss of vehicle control from loose axle clamp fasteners
A loss of vehicle control increases the risk of a crash.Microgenics Corporation recalls Thermo scientific MAS Omni CARDIO
The firm received complaints from customers reporting vial-to-vial variability when using the control with high sensitivity Troponin I assays.Siemens Healthcare Diagnostics, Inc. recalls Assay: IMMULITE 2000 Intact PTH
The potential for falsely depressed Intact PTH patient results at the low end of the assay range, less than or equal to 50 pg/mL (less than or equal to 5.3 pmol/L)…Vantive US Healthcare LLC recalls Sharesource Connectivity Platform for Use with Homechoice Claria Product Code 5CGM01…
Vantive has identified a software defect within the Sharesource Claria software, which may cause a patient s updated prescription program settings to not be properly…Cepheid recalls Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code: 07332940000158 Xpert SA…
As a result of Post-Market half-time stability testing, false negative test result was observed for a positive sample type.Greiner Bio-One North America, Inc. recalls Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%
Blood collection tubes were manufactured with the label applied too high on the tube, which shifted the printed fill level mark upward, which could result in…Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Potential issue that can cause the device to register "phantom" touches in the lower-left corner of the touchscreen during operation.MicroSurgical Technology Inc recalls MST ArcDUO 9mm
An ophthalmic knife has a suction set (not direct patient-contacting), which contains springs contaminated with an unidentified residue that may potentially cause eye…Dexcom, Inc. recalls Brand Name: Dexcom G6 Continuous Glucose Monitoring System Product Name: Dexcom G6 and…
A software defect in version v1.15.0 of the G6 Android app can cause the app to terminate unexpectedly, which may result in the user not receiving estimated glucose…Balt USA, LLC recalls Brand Name: MEGA Ballast Distal Access Platform Product Name: Mega Ballast Model/Catalog…
Due to an identified manufacturing defect involving coating material lifting within the catheter's distal inner diameter/lumen.ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection
All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured between July 31, 2023 to February 28, 2025 cause false positive results when used with Magellan…Medistim Asa recalls Brand Name: Medistim MiraQ System Product Name: Medistim MiraQ System Model/Catalog…
Printer Support Module (PSM) may be subject to insufficient soldering, which may cause loosening of the wires and system to shut down.Trividia Health, Inc. recalls Good Neighbor Pharmacy
Manufacturing defect causing LCD display issues with missing or partial segments (ghosting) that can result in misreading glucose values, potentially leading to…Aesculap Inc recalls Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER… and 3 more products
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.Beckman Coulter, Inc. recalls CellMek SPS Sample Preparation System
Automated pipetting, diluting and specimen processing workstations for flow cytometric analysis device instructions for use list incorrect dead volumes: Cassette…Surgical Theater Inc recalls SuRgical Planner and 6 more products
A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image…Canon Medical System, USA, INC. recalls VANTAGE GALAN 3T. CMSC Model: MRT-3020/U7. Model Number: MEXL-3020/B7.
Affected system contains components that do not meet the required distance between electrodes for compliance with the IEC 60601-1 standard for medical electrical…Endomagnetics LTD recalls Magseed Pro 7 cm soft tissue marker. Model Number: MS2-17-1-07. Product Description: The… and 1 more products
Potential for contamination with cotton fibers.CareFusion 303, Inc. recalls Various models of BD Pyxis Medbank: Reference numbers: 1137-00 1145-00 1146-00 1147-00… and 4 more products
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.Alcon Research LLC recalls Brand Name: Alcon Laboratories and 4 more products
Due to incomplete seals in the pouch which provide the sterile barrier.A little guidance
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Recall classes explained: Class I, II and III
What the FDA's recall classes, Canada's classes and types, and UK and EU alert levels mean, with how often each one comes up.
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How to check if your car has a recall
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What to do if something you own is recalled
Refunds, repairs, replacements and proof of destruction: what to expect, and how to handle recalled food, medicines, batteries and children's products safely.