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Medical Devices that are recalled for a defect
The following Web Notifications represents a new form of Notification for CDRH.Web Notifications are intended to augment the existing Safety Notification program and provide a mechanism to quickly disseminate device–related safety information beneficial to healthcare providers, but not appropriate for our existing forms of Notifications. Web notifications may be used in instances where the available information is limited, changing, and/or the Center may not be able to make specific recommendations, but would like to provide the information that we have to the healthcare community in a timely fashion.Web Notifications will be updated as additional information becomes available so you are encouraged to check back at this site.
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Date Issued
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Title
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| Web Notification |
12/19/2003
Updated May 7, 2004 |
Counterfeit Polypropylene Mesh |
| Web Notification |
11/25/2003 |
Updated Information for Physicians on Sub-acute Thromboses (SAT) and Hypersensitivity Reactions with Use of the Cordis CYPHER™ Sirolimus-eluting Coronary Stent |
| Web Notification |
10/29/2003 |
Information for Physicians on Sub-acute Thromboses (SAT) and Hypersensitivity Reactions with Use of the Cordis CYPHER™ Coronary Stent |
| Web Notification |
10/31/2002
Updated May 7, 2004
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Complications Related to the Use of Bone Cement and Bone Void Fillers in Treating Compression Fractures of the Spine |
| Web Notification |
10/23/2002 |
Non-Corrective Decorative Contact Lenses Dispensed Without a Prescription |
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Web Notification
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7/24/2002
Updated:
9/25/2003
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Risk of Bacterial Meningitis in Children with Cochlear Implants |
see more medical device defects at recalls.gov
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