Recalls published in August 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in August 2026, newest first.
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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
Merge PACS, medical imaging diagnostic workstation recall: Thumbnails from a previously opened patient study may be displayed
Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.
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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
United Orthopedic Corp. Brand Name: U2 Total Knee System Product Name: Femoral valgus recall: Due to an incomplete process of the component screw by a subcontractor
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
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Class II · 3 months ago
munevo Drive and munevo Drive r-net Powered Wheelchair Hands-Free recall: A software issue may cause the wheelchair's driving mechanism to fall
A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected…
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Class II · 3 months ago
Boston Scientific Corporation Radial Jaw 4 Large Capacity Biopsy Forceps recall: Potential for breach in sterile barrier of device packaging
Potential for breach in sterile barrier of device packaging.
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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
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
Pride Mobility Products Corp. Brand Name: Quantum Rehab Product Name: Quantum 4Front 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
GE Medical Systems Information Technologies Inc GE Healthcare Portrait Core Services recall: A software vulnerability may allow unauthorized persons to gain privileged
A software vulnerability may allow unauthorized persons to gain privileged access to the device, which could result in loss of patient monitoring…
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Class II · 3 months ago
Theranica Bioelectronics Ltd Nerivio Infinity. Model/ recall: Potential for the batter to have a thermal-runway event during charging
Potential for the batter to have a thermal-runway event during charging, resulting in smoke and odor.
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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
Stryker Ahto Tube SET Packaging recall: There has been an increased amount in reported complaints consistently
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
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Class II · 3 months ago
Innovasis, Inc Anti-Torque, Vector, Part: LS-749 part of Vector recall: Pedicle screw system intended to provide immobilization/stabilization
Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have…
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Class II · 3 months ago
United Orthopedic Corp. Brand Name: USTAR II Knee System Product Name: Hinge Box recall: Due to an incomplete process of the component screw by a subcontractor
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.
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Class II · 3 months ago
Stryker Ahto Dual Spike Tube SET Packaging recall: There has been an increased amount in reported complaints consistently
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
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Class II · 3 months ago
Instrumentation Laboratory GEM Premier 5000 PAK Part Numbers: 00055360010 00055360011 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 5000 lots did not meet established manufacturing…
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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
Aniara Diagnostica LLC 5-Plasma Bivalirudin AMR Verification Kit recall: Stability issues with the reconstituted lyophilized human plasma
Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a…
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Class II · 3 months ago
Copan WASP Brand Name: Wasplab Product Name: Wasplab Model/ recall: Due to a software issue within the WebApp that potentially prevents the user
Due to a software issue within the WebApp that potentially prevents the user to overwrite the results.
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Class II · 3 months ago
Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000 recall: This recall is retroactively being reported. Refurbished bassinets failed
This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution.
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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
Pride Mobility Products Corp. Brand Name: Quantum Rehab Product Name: Quantum Outback 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 3 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…