Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 2 minutes ago
United StatesNuclein LLC recalls Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument…
Due to a software issue which may result in false co-infection (e.g., Positive for Flu A, when SARS-CoV-2 is present).Therabody, Inc recalls Charger for the Therabody Theragun
Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire).Beckman Coulter Biomedical GmbH recalls REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info…
Due to software issues where does not handle combo assay results.Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence…
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.Hardy Diagnostics recalls HardyDisk AST Cefiderocol 30¿g
Due to incorrect cartridges include in affected products that there is the potential for false-susceptible or false-resistant susceptibility results and may lead to…Biofire Defense recalls FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code:
Firm has identified mismatches between the outbreak strain and the reference strain used in the development of its qualitative, multiplexed, nucleic acid-based in vitro…Boston Scientific Neuromodulation Corporation recalls INFINION CX LEAD KIT
Spinal cord stimulation system lead body may be exposed to stress at the anchor site.Merge 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.A little guidance
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