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 |
|---|---|---|---|---|
| May 11, 2017 | 1.5T Signa HDxt, 3.0T Signa HDxt, Signa HDi, Signa Vibrant Product Usage:... | Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potent... | Class II | GE Medical Systems, LLC |
| May 11, 2017 | Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system is a whol... | Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potent... | Class II | GE Medical Systems, LLC |
| May 11, 2017 | Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system is a whole... | Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potent... | Class II | GE Medical Systems, LLC |
| May 11, 2017 | Optima MR450 1.5T Product Usage: 1 .5T Brivo MR355 and 1.5T Optima MR360 ... | Possible incorrect wiring of the Uninterruptable Power Supply, which could contribute to a potent... | Class II | GE Medical Systems, LLC |
| May 8, 2017 | Merge PACS software. The firm name on the label is Merge Healthcare, Hartlan... | Merge PACS did not show unviewed images when the last view was skipped. There is a potential risk... | Class II | Merge Healthcare, Inc. |
| May 8, 2017 | Merge PACS software. Merge PACS (Picture Archiving Communication System) is... | When cut lines are shown on an image, the lines may go from being vertical and then shift to hori... | Class II | Merge Healthcare, Inc. |
| May 5, 2017 | Infant Warmer System (IWS) | GE Healthcare has recently become aware of a potential safety issue related to loose screws in t... | Class II | GE Healthcare, LLC |
| May 2, 2017 | Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1 | Carestation 620, 650 and 650c has Potential for Elevated FiCO2 and Unexpected System Malfunction | Class II | GE Healthcare, LLC |
| Apr 28, 2017 | Exact Sciences Sample Mixer 2. For In Vitro Diagnostic Use. The Exact Scien... | Exact Sciences is correcting all Sample Mixer v2 Upgrade units because of incidents of Sample Mix... | Class II | Exact Sciences Corporation |
| Apr 6, 2017 | Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite Power s... | Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8" Power Strip and TrippLi... | Class II | Merge Healthcare, Inc. |
| Mar 10, 2017 | Vivid E95/E90/E80, H45581DC, H45581LB and H45581DA. | GE Healthcare has become aware of an issue where a patient other than the intended is incorrectly... | Class II | GE Healthcare, LLC |
| Mar 10, 2017 | Vivid S60/S70/S60N/S70N, H45041SU, H45041SW, H45581MS, H45581PD. | GE Healthcare has become aware of an issue where a patient other than the intended is incorrectly... | Class II | GE Healthcare, LLC |
| Feb 6, 2017 | Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems | Reported incidents of a patient step detaching from the table. A fall from a patient step detach... | Class II | GE Healthcare, LLC |
| Jan 23, 2017 | Merge LIS | A defect in the software resulted in medications that are not associated with the patient (i.e., ... | Class II | Merge Healthcare, Inc. |
| Jan 20, 2017 | Discovery MR450 The systems are whole body magnetic resonance scanners des... | Potential safety issue with the patient bore heating on the Discovery MR450 narrow bore 1.5T MRI.... | Class II | GE Healthcare, LLC |
| Dec 9, 2016 | Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStat... | This recall has been initiated due to an issue related to the potential accidental deletion of re... | Class II | Merge Healthcare, Inc. |
| Dec 9, 2016 | Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinSt... | Merge received reports of Merge Eye Station being unable to capture images of the eye as expected... | Class II | Merge Healthcare, Inc. |
| Nov 21, 2016 | Prestige II | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | SFX | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | ADVANTX LCN+ | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | ADVANTX LCLP+ | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | Legacy | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | Innova 2000 | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | Prestilix | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | ADVANTX LCV+ | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | RFX | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | Prestige SI | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | ADVANTX LCA | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | Mallinckrodt Pharmaceuticals INOmax DSIR Plus delivery system. Model 10007. ... | Mallinckrodt discovered that some devices may have been manufactured with an out-of-tolerance man... | Class II | INO Therapeutics (dba Ikaria) |
| Nov 21, 2016 | Precision 500D | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 21, 2016 | Prestige VH | GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2,... | Class II | GE Healthcare, LLC |
| Nov 3, 2016 | GE Healthcare, Avance, Avance CS2, Amingo. | GE Healthcare has become aware of a potential safety issue where certain Avance CS2, Avance and A... | Class II | GE Healthcare, LLC |
| Oct 20, 2016 | Merge, eFilm Workstation and eFilm Lite eFilm Workstation with Modules is a... | A product issues happens for RF projection images. If user measures on RF image, .cal (Calibratio... | Class II | Merge Healthcare, Inc. |
| Sep 30, 2016 | Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecar... | GF Health Products, Inc., in conjunction with OKIN America, has initiated a voluntary field corre... | Class II | GF Health Products, Inc |
| Sep 16, 2016 | Brivo XR385, model 5215463, Digital Diagnostic Radiographic System | The placing of weight on the VRAD detector, of the Brivo XR385 digital radiographic system, can i... | Class II | GE Healthcare, LLC |
| Aug 31, 2016 | GE Healthcare SIGNA Creator, SIGNA Explorer. Diagnostic Imaging Device. | GE Healthcare is conducting a recall dealing with an incorrect RF Power Monitor Function involv... | Class II | GE Healthcare, LLC |
| Aug 4, 2016 | Infant Warmer System (IWS) | GE Healthcare has recently become aware of a potential safety issue related to loose screws in th... | Class II | GE Healthcare, LLC |
| Jul 14, 2016 | Merge RadSuite,f/k/a: Emageon Advanced Visualization , RadSuite versions 8.30... | It was reported by a customer that RadSuite images are not appearing as readable images. Thi... | Class II | Merge Healthcare, Inc. |
| Jun 17, 2016 | 3T 16ch Flex SPEEDER Coil, Large, NeoCoil Part Number NC046200, Toshiba Medic... | There is a potential for higher than specified surface temperatures involving the 3T 16ch Flex SP... | Class II | NeoCoil, LLC |
| Jun 8, 2016 | GE Healthcare, Discovery MR750w | GE Healthcare has recently become aware of a potential safety issue with the patient bore heating... | Class II | GE Healthcare, LLC |
| May 25, 2016 | iConnect Access software. The firm name on the label is Merge Healthcare, Ha... | Software displayed incorrect prior reports in the viewport area, only when more than one prior st... | Class II | Merge Healthcare, Inc. |
| May 9, 2016 | Optima 1.5T MR430s MR Scanner, a diagnostic imaging device | The gas venting may not occur properly. A site reported a magnet quenching with subsequent venti... | Class II | GE Healthcare, LLC |
| May 9, 2016 | MSK 1.5T Extreme MR Scanner, a diagnostic imaging device | The gas venting may not occur properly. A site reported a magnet quenching with subsequent venti... | Class II | GE Healthcare, LLC |
| May 9, 2016 | GE Revolution CT The system is intended for head, whole body, cardiac and ... | GEHC has become aware of a potential safety issue in the Revolution CT Patient Table that can res... | Class II | GE Healthcare, LLC |
| Apr 20, 2016 | GE, Revolution CT. The system is intended for head, whole body, cardiac, and... | An out of tolerance torque tool was used on three joints during the manufacturing process. If the... | Class II | GE Medical Systems, LLC |
| Apr 15, 2016 | GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscop... | Potential non-recoverable loss of image acquisition. The affected Discovery systems may experie... | Class II | GE Medical Systems, LLC |
| Apr 15, 2016 | Merge LIS software. The firm name on the label is Merge Healthcare. Merge... | There are potential issues with results reporting for certain run-based tests. Under certain con... | Class II | Merge Healthcare, Inc. |
| Apr 15, 2016 | GE Healthcare, Discovery IGS 740. Indicated for use in generating fluoroscop... | Potential non-recoverable loss of image acquisition. The affected Discovery systems may experie... | Class II | GE Medical Systems, LLC |
| Apr 13, 2016 | Merge Cardio software. The firm name on the label is Merge Healthcare, Hartl... | Fetal patient report was automatically pulling prior measurement data for a prior fetus since the... | Class II | Merge Healthcare, Inc. |
| Apr 8, 2016 | DR Systems Unity PACS software, now known as Merge Unity PACS | Reports were missing demographic header information when they were faxed to referring physicians. | Class II | Merge Healthcare, Inc. |
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.