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
Medtronic Perfusion Systems EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Medtronic Perfusion Systems Eopa Elongated One-Piece Arterial Cannula Blunt 22FR recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Windstone Medical Packaging, Inc. AMS Aligned Medical Solutions medical convenience recall: The recall notice was initiated due to a Medicom Urgent Medical Device
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges…
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Class II · 3 months ago
Instrumentation Laboratory Brand Name: GEM Premier 7000 with iQM3 Product Name: GEM recall: Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect…
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Class II · 3 months ago
Argon Medical Devices, Inc L-Cath Midline S/L Catheter 20ga 1mm x 20cm, REF: 384620 recall: Catheters, indicated for short/long-term peripheral access to central venous
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and…
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Class II · 3 months ago
Medtronic Perfusion Systems EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Windstone Medical Packaging, Inc. AMS Aligned Medical Solutions medical convenience recall: The recall notice was initiated due to a Medicom Urgent Medical Device
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges…
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Class II · 3 months ago
Medtronic Perfusion Systems EOPA 3D Arterial Cannula 22FR recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Philips Medical Systems IQon Spectral CT IQon Spectral CT Upgrades recall: The clinical CT scan may not automatically trigger after the Bolus Tracking
The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking…
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Class II · 3 months ago
Terex Utilities Power Over Fiber Base Module recall: Device not certified - no laser product report was filed with CDRH prior
Device not certified - no laser product report was filed with CDRH prior to distribution. Product label incorrectly states device is "Class IV"…
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Class II · 3 months ago
Windstone Medical Packaging, Inc. AMS Aligned Medical Solutions medical convenience recall: Windstone Medical Packaging recalled specific items and lots of AMS
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
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Class II · 3 months ago
Windstone Medical Packaging, Inc. AMS Aligned Medical Solutions medical convenience recall: Windstone Medical Packaging recalled specific items and lots of AMS
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
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Class II · 3 months ago
Stryker Hoffmann II Connecting Rod Micro 3 x 30mm recall: Potential cracking of the Hoffmann II Carbon Connecting Rods following
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
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Class II · 3 months ago
Windstone Medical Packaging, Inc. AMS Aligned Medical Solutions medical convenience recall: Windstone Medical Packaging recalled specific items and lots of AMS
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
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Class II · 3 months ago
Instrumentation Laboratory Brand Name: GEM Premier 5000 Product Name: GEM Premier recall: Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect…
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Class II · 3 months ago
IsoTis OrthoBiologics, Inc. OsteoBallast, 45 x 17.5 mm , REF: 56800095. Ballast recall: Demineralized bone matrix (DBM) in resorbable mesh indicated for use
Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis…
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Class II · 3 months ago
Windstone Medical Packaging, Inc. AMS Aligned Medical Solutions medical convenience recall: The recall notice was initiated due to a Medicom Urgent Medical Device
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges…
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Class I · 3 months ago
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system recall: Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and…
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Class II · 3 months ago
Instrumentation Laboratory Brand Name: GEM Premier 5000 Product Name: GEM Premier recall: Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect…
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Class II · 3 months ago
Stryker Hoffmann II Connecting Rod Micro 3 x 90mm recall: Potential cracking of the Hoffmann II Carbon Connecting Rods following
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
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Class II · 3 months ago
Medtronic Perfusion Systems EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR recall: Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia…
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Class II · 3 months ago
Stryker Hoffmann II Connecting Rod Micro 3 x 40mm recall: Potential cracking of the Hoffmann II Carbon Connecting Rods following
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
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Class II · 3 months ago
Instrumentation Laboratory Brand Name: GEM Premier 5000 Product Name: GEM Premier recall: Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect…
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Class II · 3 months ago
Windstone Medical Packaging, Inc. AMS Aligned Medical Solutions medical convenience recall: Windstone Medical Packaging recalled specific items and lots of AMS
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…