Medical Devices Recalls

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

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

Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous De...

Includes an incorrect screw seat interface.

May 6, 2026Straumann USA LLC
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 III

Heraeus, PALAMIX uno. Material Number: 66057893.

Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its lock during the mixing process. Notification is to reduce the shelf life from 3 years to 1.5 years (17 months).

May 6, 2026Heraeus Medical GmbH (Dental Division)
Medical Device
FDA DevicesClass II

Medline medical procedure kits, containing Medline Neuro Sponges (4077 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

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 III

Heraeus, PALAMIX duo. Material Number: 66057897.

Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its lock during the mixing process. Notification is to reduce the shelf life from 3 years to 1.5 years (17 months).

May 6, 2026Heraeus Medical GmbH (Dental Division)
Medical Device
FDA DevicesClass II

Medline or Centurion medical convenience kits, containing Webcol Large Alcohol P...

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 (1050 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

Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, car...

ventricular fibrillation (VF) during radiofrequency (RF) therapy with the Medtronic Sphere-9 catheter in patients who have a Biotronik Implantable Cardioverter Defibrillator (ICD) or Biotronik Cardiac Resynchronization Therapy-Defibrillator (CRT-D) implanted. The observation is caused by an interaction between the Sphere-9 catheter current flow and a safety feature built into Biotronik ICDs and CRT Ds. Medtronic recommends physicians use increased caution when using the Sphere-9 catheter for RF ablation therapy in patients implanted with a Biotronik ICD/CRT-D system, and to ensure external defibrillation systems are readily available.

May 6, 2026Medtronic, Inc.
Medical Device
FDA DevicesClass II

Philips Ingenia Elition X 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

Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model N...

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 I

Boston Scientific Cardiac Resynchronization Therapy (CRT)labeled as: 1. VALIT...

Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy pacemakers (CRT-Ps)1 and the advisory population is expanding to include all CRT-P and dual-chamber extended life (DR-EL) devices. Dual chamber modes are specifically indicated for treatment of the following: " Conduction disorders that require restoration of AV synchrony, including varying degrees of AV block " VVI intolerance (i.e., pacemaker syndrome) in the presence of persistent sinus rhythm " Low cardiac output or congestive heart failure secondary to bradycardia

May 6, 2026Boston Scientific Corporation
Medical Device
FDA DevicesClass I

Boston Scientific Pacemaker, Implantable Pulse Generator, Pacemaker (non- Cardia...

Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy pacemakers (CRT-Ps)1 and the advisory population is expanding to include all CRT-P and dual-chamber extended life (DR-EL) devices. Dual chamber modes are specifically indicated for treatment of the following: " Conduction disorders that require restoration of AV synchrony, including varying degrees of AV block " VVI intolerance (i.e., pacemaker syndrome) in the presence of persistent sinus rhythm " Low cardiac output or congestive heart failure secondary to bradycardia

May 6, 2026Boston Scientific Corporation
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

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

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204...

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

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

Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205...

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
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 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

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

Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, l...

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