Medical Devices Recalls

Defective surgical instruments, diagnostic equipment, and health device recalls.

Showing 24 of 1,658 results
Medical Device
FDA DevicesClass II

Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model ...

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

May 6, 2026Philips North America
Medical Device
FDA DevicesClass II

Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY

catheter may experience resistance when being advanced over the guidewire

May 6, 2026Merit Medical Systems, Inc.
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as fol...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as fol...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF)...

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

May 6, 2026Philips North America
Medical Device
FDA DevicesClass II

Medline and Centurion medical convenience kits, containing Webcol Large Alcohol ...

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as fol...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

i-STAT EG7+ cartridge; List Number: 03P76-25;

Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.S. marketplace may report higher than expected PCO2 and lower than expected pH results due to a manufacturing issue. A falsely high pCO2 together with a falsely low pH makes the blood gas appear as if the patient is in severe respiratory acidosis. If the clinician believes the values are real, it may trigger unnecessary or even harmful interventions such as unnecessary ventilator changes, unnecessary medications, potential harm from overcorrection, or delays in identifying true problems.

May 6, 2026Abbott Point Of Care Inc.
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as fol...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 7...

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

May 6, 2026Philips North America
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges (102 in total)

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Mesh Style Tip Protectors CSW-03-2.0 Open-end style CSW-04-4.0 Closed-end styl...

Product does not have FDA clearance.

May 6, 2026Healthmark Industries Co., Inc.
Medical Device
FDA DevicesClass II

Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. ...

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

May 6, 2026Philips North America
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as fol...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. ...

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

May 6, 2026Philips North America
Medical Device
FDA DevicesClass II

Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 7813...

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

May 6, 2026Philips North America
Medical Device
FDA DevicesClass II

Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Num...

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

May 6, 2026Philips North America
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as fol...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as fol...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline Neuro Sponges, various dimensions, labeled as: 1. Neuro Sponges, Epo...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as fol...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline and Centurion medical procedure kits, containing Medline Neuro Sponges (...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207...

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

May 6, 2026DEPUY (IRELAND)
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as fol...

During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

May 6, 2026Medline Industries, LP