The following documents have been designated “Archived” because some or all of the information in them is no longer current. They are provided for historical reference.
Date of Issue | Title | |
---|---|---|
12/11/2007 (See 9/24/08 Update) |
Deaths reported following Radio Frequency Ablation of Lung Tumors | |
2/27/2007 (See 7/16/07 Update) |
Custom Ultrasonics, Inc. Endoscope Washer/Disinfectors | |
4/18/2007 (See 4/19/07 Update) |
Possible Contamination and Malfunction of Heart Valves and Valve Conduits, Annuloplasty Rings, Surgical Grafts, Meshes and Other Devices Manufactured by Shelhigh, Inc. See Related Document: Advice to Patients |
|
4/28/2006 | Important Safety Recommendations for Baxter's COLLEAGUE Infusion Pumps | |
12/20/2005 (See 2/1/07 Update) |
Update of Information about Ralstonia spp. Associated with Vapotherm® Respiratory Gas Administration Device | |
4/24/2006 (See 6/19/06 Update) |
Oxygen Regulator Fires Resulting from Incorrect Use of CGA 870 Seals | |
4/21/2006 (See 5/31/06 Update) |
Fungal Keratitis Infections Related to Contact Lens Use (First Update) |
|
4/10/2006 (See 5/31/06 Update) |
Fungal Keratitis Infections Related to Contact Lens Use |
|
10/27/2005 | New Information about Ralstonia spp. Associated with Vapotherm® Respiratory Gas Administration Device | |
10/14/2005 | Recall of Boston Scientific ENTERYX® Procedure Kits and ENTERYX® Injector Single Packs for Treatment of Gastroesophageal Reflux Disease (GERD) |
|
8/23/2005 (See 2/27/06 Update) |
Gambro Prisma® Continuous Renal Replacement System | |
7/24/2002 Updated: 9/25/2003 |
Risk of Bacterial Meningitis in Children with Cochlear Implants | |
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 | |
10/29/2003 | Information for Physicians on Sub-acute Thromboses (SAT) and Hypersensitivity Reactions with Use of the Cordis CYPHER™ Coronary Stent | |
8/21/2002 | Human Tissue Processed by Cryolife, Inc | |
3/15/2002 | Recall of Ob/Gyn and Surgical Products Manufactured by A & A Medical/Rocket USA/Lifequest | |
3/29/2000 | Recall of Clinipad Sterile Products Used in Prepackaged Procedure Kits and Trays | |
12/30/1999 | Important Information Regarding the Year 2000 Transition | |
12/13/1999 | FDA Public Health Notification: Important Information about Y2K and Medical Devices | |
7/16/1999 | Important Y2K Planning Information | |
12/29/1998 | FDA Medical Device Malfunction | |
10/14/1998 | Interaction Between Minute Ventilation Rate-Adaptive Pacemakers and Cardiac Monitoring and Diagnostic Equipment | |
8/5/1997 | Update to Radioactivity in Radiation Protection Devices | |
6/13/1997 | Radioactivity in Radiation Protection Devices | |
10/11/1995 | Urgent Notice About Recalled Blood-Glucose Test Strips | |
1/26/1994 | Laerdal Defibrillators | |
8/20/1992 | Important Information About Rophae Intraocular Lenses | |
3/28/1985 | Defibrillator Batteries | |
7/2/1984 | Pediatric Cribs |
Updated September 24, 2008
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