Browse Device Recalls
922 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 922 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 922 FDA device recalls in WI.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Oct 19, 2012 | Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard Endo... | Titan Spine LLC, is conducting a recall on the Endoskeleton TA VBR products. The labeling accompa... | Class II | TITAN SPINE, LLC |
| Oct 15, 2012 | GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The T-piece... | Oxygen and air wall inlet fittings on the back panel of the resuscitation systems were reversed d... | Class I | GE Healthcare, LLC |
| Oct 15, 2012 | Giraffe and Panda Bag and Mask Resuscitation System The T-piece Resuscitat... | Oxygen and air wall inlet fittings on the back panel of the resuscitation systems were reversed d... | Class I | GE Healthcare, LLC |
| Oct 12, 2012 | GE Discovery NM/CT670; GE Discovery NM 630 Product Usage: a medical too... | GE Healthcare has recently become aware of a potential safety issue associated with the table pa... | Class II | GE Healthcare, LLC |
| Oct 5, 2012 | Pinnacle3 VCC P/N 4598 001 41341 REV A, Philips Medical Systems (Cleveland), ... | Philips Medical Systems Cleveland), Inc. is recalling Pinnacle3 Virtual Client Connection softwa... | Class II | Philips Medical Systems (Cleveland), Inc. |
| Sep 26, 2012 | GE Healthcare Definium 5000/5220493-2 X-Ray System | When quickly switching the protocols from AEC to Fixed under the same view, if the user selection... | Class II | GE Healthcare, LLC |
| Sep 26, 2012 | GE Healthcare Definium 5000 / 5220493 X-Ray System | When quickly switching the protocols from AEC to Fixed under the same view, if the user selection... | Class II | GE Healthcare, LLC |
| Sep 20, 2012 | GE Healthcare Optima 200amx Mobile general purpose radiographic imaging of... | It was discovered GE Healthcare has become aware of a firmware issue on the mobile radiographic p... | Class II | GE Healthcare, LLC |
| Sep 20, 2012 | GE Healthcare Optima XR 200amx with digital upgrade Mobile general purpose... | It was discovered GE Healthcare has become aware of a firmware issue on the mobile radiographic p... | Class II | GE Healthcare, LLC |
| Sep 20, 2012 | GE Healthcare Optima XR 220amx Mobile general purpose radiographic imaging... | It was discovered GE Healthcare has become aware of a firmware issue on the mobile radiographic p... | Class II | GE Healthcare, LLC |
| Sep 20, 2012 | GE Healthcare, Seno Advantage, 5183685, 5183685-2, 5183685-3, 5183685-4, 5183... | GE Healthcare has recently become aware that patient mismatch without a warning message could occ... | Class II | GE Healthcare, LLC |
| Sep 20, 2012 | GE Healthcare Brivo XR 285 Mobile general purpose radiographic imaging of ... | It was discovered GE Healthcare has become aware of a firmware issue on the mobile radiographic p... | Class II | GE Healthcare, LLC |
| Aug 16, 2012 | GE Healthcare, Innova 2121IQ, Innova 3131IQ Cardiovascular X-ray imaging syst... | GE Healthcare has recently become aware of a potential safety issue with respect to the Innova 21... | Class II | GE Healthcare, LLC |
| Aug 13, 2012 | GE Healthcare, LOGIQ S8 Ultrasound System The device is intended for use ... | GE Healthcare became aware of a potential issue related to incorrect image measurement associated... | Class II | GE Healthcare, LLC |
| Aug 7, 2012 | GE Healthcare, Optima XR220amx, Optima XR200amx, and Brivo XR285amx. The s... | GE Healthcare conducted a recall on various mobile x-ray units (Optima XR220amx, Optima XR200amx,... | Class II | GE Healthcare, LLC |
| Aug 3, 2012 | GE Healthcare Brivo XR385 DR-F/ X-Ray System X-Ray System | GE Healthcare has become aware of a software issue on the interface of the Brivo XR385 DR-F/ Mode... | Class II | GE Healthcare, LLC |
| Aug 1, 2012 | GE Healthcare Optima XR 220amx 15kw Mobile X-Ray System The GE Automatic M... | GE Healthcare has become aware of a software issue on the interface of the mobile radiographic pr... | Class II | GE Healthcare, LLC |
| Aug 1, 2012 | GE Healthcare Optima XR 200 amx with Digital Upgrade. The GE Automatic Mob... | GE Healthcare has become aware of a software issue on the interface of the mobile radiographic pr... | Class II | GE Healthcare, LLC |
| Aug 1, 2012 | GE Healthcare Optima XR 220amx 30kw Mobile X-ray System The GE Automatic M... | GE Healthcare has become aware of a software issue on the interface of the mobile radiographic pr... | Class II | GE Healthcare, LLC |
| Jul 20, 2012 | CARESCAPE Monitor B850 Product Usage: The CARESCAPE TM Monitor B850 is ... | GE Healthcare become aware of 4 potential issues associated with the CARESCAPE Monitor B850. The... | Class II | GE Healthcare, LLC |
| Jul 13, 2012 | GE Healthcare, VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM. ... | GE Healthcare has recently become aware that during use of the Voluson E6 or E8 systems, that an ... | Class II | GE Healthcare, LLC |
| Jul 12, 2012 | GE Healthcare, CARESCAPE Monitor B650. The CARESCAPE Monitor B650 is a mul... | GE Healthcare has recently become aware of a number of potential issues associated with the CARE... | Class II | GE Healthcare, LLC |
| Jul 10, 2012 | Optima XR200amx. Mobile general purpose radiographic imaging of the human he... | Software issue: a violation of 21 CFR 1020.31(a). After an image is taken, when the user selects... | Class II | GE Healthcare, LLC |
| Jul 10, 2012 | Optima XR220amx Mobile general purpose radiographic imaging of the human h... | Software issue: a violation of 21 CFR 1020.31(a). After an image is taken, when the user selects... | Class II | GE Healthcare, LLC |
| Jul 2, 2012 | Merge HEMO software. | The International Normalized Ratio (INR) value displayed in the study report does not match the v... | Class II | Merge Healthcare, Inc. |
| Jun 28, 2012 | GE Healthcare, AW Server. Product Usage: . AW Server is a medical softwar... | GE Healthcare has recently become aware of a potential safety issue with respect to the Results V... | Class II | GE Healthcare, LLC |
| Jun 26, 2012 | GE Healthcare, Dash 3000/4000/5000. The Dash 3000/4000/5000 patient monito... | GE Healthcare has recently become aware of a potential issue due to an unexpected loss of Custom ... | Class II | GE Healthcare, LLC |
| Jun 26, 2012 | GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece Neonatal... | Disposable T-Piece circuits used with resuscitation systems are unable to achieve maximum Peak In... | Class I | GE Healthcare, LLC |
| Jun 13, 2012 | GE Healthcare, Dash 3000, Dash 4000 and Dash 5000 Physiological Patient Monit... | GE has become aware of multiple issues affecting the Dash 3000/4000/5000 Patient Monitor. The... | Class II | GE Healthcare, LLC |
| Jun 13, 2012 | GE Healthcare, Dash Port 2 Docking Station. Product Usage: is a docking st... | GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and DashPort 2 monitor.... | Class II | GE Healthcare, LLC |
| Jun 12, 2012 | GE Healthcare, Invasive Blood Pressure Care Cables. Product ID Number: 201... | GE Healthcare has become aware through complaints of a potential safety issue with its Invasive B... | Class II | GE Healthcare, LLC |
| Jun 8, 2012 | GE Healthcare, Discovery MR750, Discovery 450, Optima 450W (with and without ... | GE Healthcare has recently become aware of a Reformat Image Flip Issue associated with GE MR Prod... | Class II | GE Healthcare, LLC |
| Jun 8, 2012 | GE Healthcare, GE 1.5T SIGNA HDe MR SYSTEM. Indicated for use as a diagnos... | GE Healthcare has recently become aware of a Reformat Image Flip Issue associated with GE MR Prod... | Class II | GE Healthcare, LLC |
| Jun 8, 2012 | GE Healthcare, Optima MR360/Brivo MR355 (HDsv), GE 0.35T Signa Ovation HD MR ... | GE Healthcare has recently become aware of a Reformat Image Flip Issue associated with GE MR Prod... | Class II | GE Healthcare, LLC |
| May 29, 2012 | Advantage Workstation Volume Share 2 (versionAW4.4_04) with Volume Viewer 3 a... | GE Healthcare has became aware of two issues with the Advantage Workstation. 1) A possible mis... | Class II | GE Healthcare, LLC |
| May 25, 2012 | GE Healthcare Volume Viewer Plus 5.x (Advantage Workstation 4.2) Volume Vie... | Incorrect views and measurements possible. GE Healthcare became aware of multiple potential safe... | Class II | GE Healthcare, LLC |
| May 24, 2012 | GE Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage 2.1 Seno Advanta... | GE Healthcare has become aware of an issue associated with the magnification images acquired on n... | Class II | GE Healthcare, LLC |
| May 24, 2012 | GE Healthcare Advantage Workstations, Advantage Worksation version 4.2 and 4.... | GE Healthcare is informing you of incorrect measurements when using the Aorta analysis protocol o... | Class II | GE Healthcare, LLC |
| May 24, 2012 | AdvantageSim MD versions 7.4 through 7.6, Model 5160092-2 Version 7.4, 516009... | It was reported by a customer site that when using GE AdvantageSim MD on Advantage Workstation, t... | Class II | GE Healthcare, LLC |
| May 24, 2012 | GE Healthcare, Seno Advantage 2.2 workstations with software version 22_01 an... | GE Healthcare has recently become aware of inaccurate Scale factor annotation provided by SenoAdv... | Class II | GE Healthcare, LLC |
| May 24, 2012 | GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume View... | GE Healthcare has become aware of a potential safety issue due to incorrect alignment of fused CT... | Class II | GE Healthcare, LLC |
| Apr 23, 2012 | GE Healthcare, Discovery MR750w 3.0T System. Part Number: 5352293. Produ... | GE Healthcare has recently become aware of a potential issue due to image flip in frequency encod... | Class II | GE Healthcare, LLC |
| Apr 10, 2012 | The brand name of the device is Laser Loupes, a dentalloupe with laser eye ... | The firm initiated the recall for Laser Loupes because the ink used to mark which laser frequency... | Class II | Kerr Corporation |
| Apr 10, 2012 | GE Healthcare, Aestiva/5 7900 SmartVent, anesthesia machine. Used in Datex-O... | GE Healthcare has recently become aware of a potential safety issue due to the interlock slide me... | Class I | GE Healthcare, LLC |
| Apr 4, 2012 | GE Healthcare Optima Mobile X-ray System. The GE Automatic Mobile X-Ray (A... | GE Healthcare has become aware of a software issue on the interface of the mobile radiographic pr... | Class II | GE Healthcare, LLC |
| Mar 27, 2012 | GE Healthcare, Advantage Workstation, READY View Application. Image analys... | GE Healthcare has become aware that when analyzing fMRI images using the READY View application s... | Class II | GE Healthcare, LLC |
| Mar 6, 2012 | GE Healthcare Quasar Nuclear Medicine System, Hawkeye Option and Hawkeye 4 Op... | Accelerated fatigue of the lateral axis motion subsystem of the Infinia Computed Emission Tomogra... | Class II | GE Healthcare, LLC |
| Feb 17, 2012 | GE Healthcare Carescape Patient Data Module with v2.0 software used with Sola... | GE Healthcare became aware of two issues with the Patient Data Module using Version 2.0 software ... | Class II | GE Healthcare, LLC |
| Jan 23, 2012 | VMX, VMX Plus Mobile Radiographic Unit with the following models: 45296139;... | GE Healthcare has become aware of an issue associated with the base casting for the articulated a... | Class II | GE Healthcare, LLC |
| Jan 4, 2012 | GE Healthcare Muse v7 cardiology information system. Model number 2026443-00... | GE Healthcare conducted a recall on the Muse v7 because incorrect medications were displayed on ... | Class II | GE Healthcare, LLC |
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.