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.
3,851 recalls, newest first · Checked 9 minutes ago
United StatesMerge Healthcare, Inc. recalls Merge PACS and 1 more products
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.Munevo GMBH recalls munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control…
A software issue may cause the wheelchair's driving mechanism to fall out of calibration.Biomet, Inc. recalls Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description… and 4 more products
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging…GE Medical Systems Information Technologies Inc recalls GE Healthcare Portrait Core Services SW V 1.2.0
A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring, missed patient…Theranica Bioelectronics LTD recalls Nerivio Infinity. Model/Catalog Number: FGD000100. Software Version: FW Version 4.1.2.0
Potential for the batter to have a thermal-runway event during charging, resulting in smoke and odor.Innovasis, Inc recalls Anti-Torque
Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque…Stryker Corporation recalls STRYKER AHTO TUBE SET PACKAGING and 4 more products
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.Instrumentation Laboratory recalls GEM Premier 7000 with iQM3 Part Numbers: 00077407508 00077407510 00077415004 00077415008… and 1 more products
The active ingredient concentration in the lysing bag solution of specific GEM Premier 7000 with iQM3 PAK lots did not meet established manufacturing specifications.Aniara Diagnostica LLC recalls 5-PLASMA Bivalirudin AMR Verification Kit and 2 more products
Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified.Copan WASP recalls Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version…
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.Happiest Baby, Inc recalls Happiest Baby
This recall is retroactively being reported.Tissium Sa recalls Brand Name: COAPTIUM Connect Product Name: COAPTIUM Connect Model/Catalog Number… and 7 more products
Currently labeled shelf life of 36 months is not substantiated by real-time data.Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum… and 12 more products
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use.Boston Scientific Corporation recalls Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN… and 2 more products
Potential for breach in sterile barrier of device packaging.AVID Medical, Inc. recalls Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle… and 2 more products
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of…United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: Femoral offset bushing and 1 more products
Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.Freudenberg Medical, LLC recalls Blom-Singer Classic Indwelling Voice Prosthesis and 1 more products
Incorrect labeling- The labeled box for the Large Esophageal Flange contains a Large Esophageal and Tracheal Flange, and the labeled box for the Large Esophageal and…Beckman Coulter Inc. recalls REF # D23352 and 1 more products
Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."GE Medical Systems Information Technologies Inc recalls GE Healthcare MAC VU360
Software issue issue with the MAC VU360 v3.0 system.Integrated Medcraft LLC recalls FORWARD Oral Airway Kit and 1 more products
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.Oxos Medical Inc recalls Brand Name: OXOS Medical
Due to a defective circuit board that overheatsSiemens Healthcare Diagnostics, Inc. recalls Atellica CH Urine Albumin REF: 11537225
Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely depressed…United Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: PSA Box Trial and 3 more products
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.A little guidance
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