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 23 minutes ago
United StatesAVID Medical, Inc. recalls Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH31. and 1 more products
A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications.Philips North America recalls Philips Smart-hopping 2.0 AP 1.4 GHz
Unreliable wireless roaming behavior of Smart-hopping 1.0 wireless clients during transport when connecting to Smart-hopping 2.0 infrastructure, resulting in loss of…Axonics, Inc. recalls PNE Lead Implant Kit REF: 1701
Retroactively Reported: 10mL luer lock syringes included in kit may leak , break or experience other issues that may pose a risk to users.B Braun Medical Inc recalls B Braun SAFSITE Injection Site
Potential for leakage and backflow at the Safsite valve.Think Surgical, Inc. recalls Think Surgical Square Driver REF: 109126
Robotic system square drive failed to meet design specifications potentially resulting in pin becoming stuck in square driver or the pin wobbling during drilling.Medtronic MiniMed, Inc. recalls CareLink Clinic
CareLink Clinic software version 4.4A includes a software defect in the Settings Calculator feature in which the calculation logic fails to use custom values entered by…Medtronic Neuromodulation recalls InterStim SureScan MRI Leads 978A1 & 978B1: LEAD 978A128 ISTM MICRO 28CM SSMRI TINED… and 1 more products
Wrong lead or percutaneous extension selected.Beckman Coulter, Inc. recalls ROTOR ASSY-SW40 and 1 more products
Optima XE XPN ultracentrifuge rotors may contain a microstructure defect that can cause rotors to break into two or more pieces (bifurcate) during a centrifugation run…Techno-Path Manufacturing LTD. recalls Techno-Path Multichem AE Unassayed Level 1 REF:AE621X and 2 more products
A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material.Medtronic MiniMed, Inc. recalls Generic Name: MiniMed Go App Generic Name: MiniMed Go App Model/Catalog Number: MMT-8600
A software defect in which existing users who had previously configured and enabled the long-acting dose reminder feature in version 1.2.0 or earlier experienced…Greiner Bio-One North America, Inc. recalls Brand Name: VACUETTE Product Name: LH Lithium Heparin Separator Model/Catalog Number…
Lot B26043FM may include EDTA contamination which introduces potassium while chelating calcium in patient samples, leading to falsely elevated potassium (K+) and…Medline Industries, LP recalls MEDLINE DRAPE C-SECTION W/POUCH ST 7/CS and 12 more products
Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.Medtronic Navigation, Inc. recalls Medtronic NDI Passive Spheres REF: 8801071 and 3 more products
Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect and track…Ventec Life Systems, Inc. recalls VOCSN+Pro and 11 more products
Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.Life Technologies Holdings Pte Ltd recalls Ion Torrent Genexus Dx with software
DNA or RNA sequencing system software has vulnerabilities.Boston Scientific Cork, Ltd. recalls Direxion Torqueable Microcatheter and 40 more products
The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and…Right Value Drug Stores LLC recalls Testosterone Cypionate
Lack of sterility assurance.Ascend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets
Out of specification due to dissolution.Pfizer recalls Levoxyl and 1 more products
Subpotent Drug: confirmed out-of-specification (OOS) assay during stability testing.AvKARE recalls Amitriptyline Hydrochloride
Failed dissolution specifications.Greenwich Rx recalls Glutathione Injection
Microbial Contamination of Sterile ProductsViatris, Inc. recalls Telmisartan and Amlodipine
Superpotent Drug: potential for the Telmisartan content in these lots to exceed specificationsShenzhen Techdow Pharmaceutical Co., Ltd. recalls Heparin Sodium Injection
Lack of Assurance of SterilityA little guidance
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