Browse Device Recalls
3,276 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 3,276 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.
Medical Device Recalls
Browse 3,276 FDA device recalls in 2024.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Jan 3, 2024 | Neurovascular embolization device. The Optima Coil System is a series special... | Discoloration was identified along the delivery pusher which was attributed to corrosion of the h... | Class II | BALT USA, LLC |
| Jan 3, 2024 | Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the follow... | Their is a potential that the implant curved stem may be oriented incorrectly. | Class II | United Orthopedic Corporation |
| Jan 3, 2024 | Intera Achieva 1.5T Pulsar. Model (REF) Number 781171. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference N... | Their is a potential that the implant curved stem may be oriented incorrectly. | Class II | United Orthopedic Corporation |
| Jan 3, 2024 | Achieva 1.5T Initial system. Model (REF) Numbers 781178. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | Synapse CV 6. with AR. A web-based application as the primary user interfa... | The LV Mass (2D Bullet) equation may be calculated incorrectly, resulting in a variance in the ma... | Class II | FUJIFILM Healthcare Americas Corporation |
| Jan 3, 2024 | Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137; ... | A software error caused an increase in tray gripper motion errors that causes intermittent hard s... | Class II | Beckman Coulter, Inc. |
| Jan 3, 2024 | Achieva XR. Model (REF) Numbers 781153, 781253. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | Synapse Cardiology PACS V7.3.0, V7.2, V7.1, V7.0. A web-based application a... | The LV Mass (2D Bullet) equation may be calculated incorrectly, resulting in a variance in the ma... | Class II | FUJIFILM Healthcare Americas Corporation |
| Jan 3, 2024 | Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DW... | The incorrect device is contained in the labeled package. | Class II | Tornier, Inc |
| Jan 3, 2024 | 1. HeartMate Touch Communication System, REF HMT1100 2. HeartMate Touch Comm... | Due to software and controller systems that results in unexpected pump start or pump stop. | Class I | Thoratec Corp. |
| Jan 3, 2024 | Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270, 782113, 782... | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 3, 2024 | The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a... | One lot of the Sofia 2 Flu + SARS Antigen FIA (Lot 709083) was labelled with incorrect expiration... | Class II | Quidel Corporation |
| Jan 3, 2024 | Intera 1.5T Achieva Nova. Model (REF) Numbers 781172. | The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in cont... | Class II | Philips North America |
| Jan 2, 2024 | Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically t... | Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may stop functioning and ... | Class II | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Jan 2, 2024 | Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically t... | Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible... | Class II | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Jan 2, 2024 | Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the D... | Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible... | Class II | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Jan 2, 2024 | 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier | Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1... | Class II | Zimmer Surgical Inc |
| Jan 2, 2024 | Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically t... | Framegrabber card may not perform as intended. Monitor may show no viewports, or show one or more... | Class II | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Jan 2, 2024 | Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the D... | Framegrabber card may not perform as intended. Monitor may show no viewports, or show one or more... | Class II | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
Frequently Asked Questions
When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.
All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.
Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.