Browse Device Recalls
12 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 12 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 12 FDA device recalls in 2007.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Nov 19, 2007 | OEC 8800 Flexiview designed to provide fluoroscopic and spot-film imaging of ... | Please be aware that this is not a new recall. The firm has taken action; but, due to administra... | Class II | GE OEC Medical Systems, Inc |
| Nov 19, 2007 | OEC 9900 Elite, OEC 9900 Elite MD Motorized C-arm System, OEC 9900 Elite NAV ... | Please be aware that this is not a new recall. The firm has taken action; but, due to administra... | Class II | GE OEC Medical Systems, Inc |
| Nov 19, 2007 | OEC 9800, OEC FluoroTrak 9800 Plus, OEC 9800 Plus, OEC 9800 MD Motorized C-ar... | Please be aware that this is not a new recall. The firm has taken action; but, due to administra... | Class II | GE OEC Medical Systems, Inc |
| Oct 29, 2007 | Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model... | The power to the Esprit Display's Backlight is interrupted, causing the GUI to flicker or go dark... | Class II | Respironics California Inc |
| Oct 19, 2007 | GEHC OEC 8800 Mobile Fluoroscopic X-ray System, GE Healthcare, Surgery, Salt ... | X-ray units did not meet manufacturer's specification for linearity. | Class II | GE OEC Medical Systems, Inc |
| Sep 14, 2007 | HiRes 90K devices with Helix Electrodes Model CI 1400-02H The HiResolution... | Advanced Bionics is recalling the the HiRes 90K cochlear implant with HiFocus Helix Electrode bec... | Class II | Advanced Bionics Corporation |
| Apr 2, 2007 | Radiological Image Processing System The system is an aid to locate anatom... | The FluoroTrak Spinal Navigation Application on the OEC 9900 EliteNAV could result in an incorrec... | Class I | GE OEC Medical Systems, Inc |
| Mar 27, 2007 | OEC 9800 Plus Digital; MDL number A349855. Product Usage: Is designed to ... | Please be aware that this is not a new recall. The firm has taken action; but, due to administra... | Class II | GE OEC Medical Systems, Inc |
| Mar 27, 2007 | UroView 2800; MDL number A349855. Product Usage: Designed to provide fluor... | Please be aware that this is not a new recall. The firm has taken action; but, due to administra... | Class II | GE OEC Medical Systems, Inc |
| Mar 27, 2007 | OEC MiniView 6800 Mobile; MDL number A349855. Product Usage: The mini 680... | Please be aware that this is not a new recall. The firm has taken action; but, due to administra... | Class II | GE OEC Medical Systems, Inc |
| Jan 18, 2007 | Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocol... | Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labele... | Class II | Beevers Manufacturing & Supply, Inc. |
| Jan 9, 2007 | No packaging. The device is a computed tomography scanner. Intended to ... | When the Extended Display Firled ov View reconstruction is used, the CT numbers and anatomy in te... | Class II | Philips Medical Systems (Cleveland) 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.