Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 150mm recall — FDA Z-2833-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
August 2026 recalls — page 12
These records include useful source details for the selected month.
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 120mm recall — FDA Z-2832-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceAug 5, 2026
PHILIPS MEDICAL SYSTEMS Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance recall — FDA Z-2650-2026
The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS
Medical DeviceAug 5, 2026
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3 recall — FDA Z-2795-2026
This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall…
Class IIFDA: OngoingPermobil Inc
Medical DeviceAug 5, 2026
Medtronic Perfusion Systems EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR, intended recall — FDA Z-2808-2026
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation,…
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceAug 5, 2026
Medtronic Perfusion Systems EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended recall — FDA Z-2806-2026
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation,…
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2799-2026
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed Neurological Sponges Non-Sterile Models 55992C to 55998C due to…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceAug 5, 2026
GEM Premier 7000 with iQM3 recall — FDA Z-2822-2026
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 patient ID.
Class IIFDA: OngoingInstrumentation Laboratory
Medical DeviceAug 5, 2026
Argon Medical Devices L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620 recall — FDA Z-2804-2026
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or…
Class IIFDA: OngoingArgon Medical Devices, Inc.
Medical DeviceAug 5, 2026
Medtronic Perfusion Systems EOPA 3D Arterial Cannula DIL TIP 22FR, intended for use with recall — FDA Z-2810-2026
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation,…
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2801-2026
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed Neurological Sponges Non-Sterile Models 55992C to 55998C due to…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceAug 5, 2026
Medtronic Perfusion Systems EOPA 3D Arterial Cannula 22FR, intended for use with recall — FDA Z-2811-2026
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation,…
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceAug 5, 2026
PHILIPS MEDICAL SYSTEMS IQon Spectral CT IQon Spectral CT Upgrades recall — FDA Z-2651-2026
The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS
Medical DeviceAug 5, 2026
Terex Utilities Power Over Fiber Base Module recall — FDA Z-2745-2026
Device not certified - no laser product report was filed with CDRH prior to distribution. Product label incorrectly states device is "Class IV", although Class 1 is appropriate for device.…
Class IIFDA: OngoingTerex Utilities
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2817-2026
Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2816-2026
Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 30mm recall — FDA Z-2827-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2819-2026
Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceAug 5, 2026
GEM Premier 5000 recall — FDA Z-2824-2026
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 patient ID.
Class IIFDA: OngoingInstrumentation Laboratory
Medical DeviceAug 5, 2026
IsoTis OrthoBiologics OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095 recall — FDA Z-2820-2026
Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with approx. 4.5 cc DBM…
Class IIFDA: OngoingIsoTis OrthoBiologics, Inc.
Medical DeviceAug 5, 2026
Windstone Medical Packaging AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled recall — FDA Z-2800-2026
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed Neurological Sponges Non-Sterile Models 55992C to 55998C due to…
Class IIFDA: OngoingWindstone Medical Packaging, Inc.
Medical DeviceAug 5, 2026
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous recall — FDA Z-2735-2026
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy.
Class IFDA: OngoingResMed Ltd.
Medical DeviceAug 5, 2026
GEM Premier 5000 recall — FDA Z-2823-2026
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 patient ID.
Class IIFDA: OngoingInstrumentation Laboratory
Medical DeviceAug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 90mm recall — FDA Z-2831-2026
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
Class IIFDA: OngoingStryker GmbH
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.