Latest recalls — page 49
Older notices, newest first.
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Class III · 3 months ago
Siemens Healthcare Diagnostics, Inc. Syva Emit Disopyramide Assay Enzyme Immunoassay recall: Out-of-specification sodium azide concentration in Syva Emit Disopyramide
Out-of-specification sodium azide concentration in Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1. While the assay results were not…
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Class II · 3 months ago
Philips Azurion under the following System Descriptions recall: Potential Loss of imaging functionality, loss of motorized movement
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
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Class II · 3 months ago
Contego Medical, Inc Neuroguard IEP 3 in 1 recall: Carotid stent and post-dilation balloon system with integrated embolic
Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter, that due to a wire-to-filter-bond…
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Class II · 3 months ago
Instrumentation Laboratory GEM Premier 7000 with iQM3 Part Numbers: 00077407508 recall: The active ingredient concentration in the lysing bag solution of specific
The active ingredient concentration in the lysing bag solution of specific GEM Premier 7000 with iQM3 PAK lots did not meet established manufacturing…
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Class I · 3 months ago
AVID Medical, Inc. Halyard convenience kits containing recalled Medline Namic recall: Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates…
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Class II · 3 months ago
Philips Allura, Cardio Vascular-Allura Centron recall: Potential Loss of imaging functionality, loss of motorized movement
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
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Class II · 3 months ago
Beckman Coulter Inc. REF # D23352, MicroScan LabPro V5.03 Panel Update 11 recall: Analyzers contain incorrect algorithms which may affect antimicrobial
Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."
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Class II · 3 months ago
Nuclein LLC Brand Name: Dash Rapid PCR Instrument Product Name: Dash Rapid PCR recall: Due to a software issue which may result in false co-infection (e.g
Due to a software issue which may result in false co-infection (e.g., Positive for Flu A, when SARS-CoV-2 is present).
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Class II · 3 months ago
Charger for the Therabody Theragun, G4 PRO massage device recall: Charging cradle for the device may overheat while charging the device's
Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire). Firm has…
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Class II · 3 months ago
Beckman Coulter Biomedical GmbH Remisol Advance with Software Version 2.5 Udi-Di recall: Due to software issues where does not handle combo assay results
Due to software issues where does not handle combo assay results. The software may replace the final combo test result with one of the sub-results…
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Class II · 3 months ago
Pride Mobility Products Corp. Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Model/ recall: If the "Remind Me Later" option is selected for user reminders
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs…
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Class II · 3 months ago
Brand Name: Medical Action Industries Product Name: Dialysis Change recall: Convenience kits contain needle free access device that has an improper seal
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
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Class II · 3 months ago
Pride Mobility Products Corp. Brand Name: Quantum Rehab Product Name: R-TRAK Model/ recall: If the "Remind Me Later" option is selected for user reminders
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs…
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Class II · 3 months ago
Biomet, Inc. Intramedullary Bone Saw Blade Assembly Model/ recall: Zimmer Biomet is conducting a medical device recall removal for various sizes
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile…
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Class II · 3 months ago
Tissium Sa Brand Name: Coaptium Connect Product Name: Coaptium Connect Model/ recall: Currently labeled shelf life of 36 months is not substantiated by real-time
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26…
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Class II · 3 months ago
HardyDisk AST Cefiderocol 30¿g REF Z9435 HardyDisk AST Cefiderocol 30¿g recall: Due to incorrect cartridges include in affected products that there
Due to incorrect cartridges include in affected products that there is the potential for false-susceptible or false-resistant susceptibility results…
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Class II · 3 months ago
Pride Mobility Products Corp. Brand Name: Quantum Rehab Product Name: Quantum Rival recall: If the "Remind Me Later" option is selected for user reminders
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs…
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Class II · 3 months ago
Pride Mobility Products Corp. Brand Name: Quantum Rehab Product Name: Q6 Edge HD recall: If the "Remind Me Later" option is selected for user reminders
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs…
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Class II · 3 months ago
Tissium Sa Brand Name: Coaptium Connect Product Name: Coaptium Connect Model/ recall: Currently labeled shelf life of 36 months is not substantiated by real-time
Currently labeled shelf life of 36 months is not substantiated by real-time data. Devices will be relabeled to reflect revised shelf life of 26…
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Class II · 3 months ago
Biofire Defense FilmArray Ngds Warrior Panel REF Ngds-Asy-0007 Udi-Di code recall: Firm has identified mismatches between the outbreak strain and the reference
Firm has identified mismatches between the outbreak strain and the reference strain used in the development of its qualitative, multiplexed, nucleic…
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Class I · 3 months ago
Boston Scientific Neuromodulation Corporation Infinion CX Lead KIT, 50CM recall: Spinal cord stimulation system lead body may be exposed to stress
Spinal cord stimulation system lead body may be exposed to stress at the anchor site. This may result in high impedance measurements or lead…
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Class II · 3 months ago
Pride Mobility Products Corp. Brand Name: Quantum Rehab Product Name: Quantum 1450 recall: If the "Remind Me Later" option is selected for user reminders
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs…
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Class II · 3 months ago
Pride Mobility Products Corp. Brand Name: Quantum Rehab Product Name: 4Front Model/ recall: If the "Remind Me Later" option is selected for user reminders
If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs…
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Class II · 3 months ago
Biomet, Inc. Intramedullary Bone Saw Blade Assembly Model/ recall: Zimmer Biomet is conducting a medical device recall removal for various sizes
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile…