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Medical Device Recalls

Drug and Medical Recalls

View the list below of the latest Medical Device Recall information. The majority of the recalls below originated from either the FDA or the USDA.

106 total items found
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Covidien Initiates Voluntary Recall of Pre-Filled Syringes Containing Heparin

Recall Date: Friday, March 28th, 2008

Actavis Recalls Remaining Fentanyl Patches in the US as Precaution

Recall Date: Saturday, March 1st, 2008

Baxter to Proceed with Recall of Remaining Heparin Sodium Vial Products

Recall Date: Thursday, February 28th, 2008

Actavis Recalls Certain Fentanyl Patches in the US as Precaution

Recall Date: Sunday, February 17th, 2008

PRICARA™ RECALLS 25 mcg/hr DURAGESIC® (fentanyl transdermal system) CII PAIN PATCHES

Recall Date: Tuesday, February 12th, 2008

Baxter Issues Urgent Nationwide Voluntary Recall of Heparin 1,000 Units/ml 10 and 30ml Multi-Dose Vials

Recall Date: Friday, January 25th, 2008

B. Braun´s Supplier Prompts Voluntary Recall of All Lots and All Sizes of Pre-Filled Heparin and Normal Saline Flush Syringes

Recall Date: Friday, January 18th, 2008

AM2 PAT, Inc. Issues Nationwide Recall of All Lots and All Sizes of Pre-Filled Heparin and Normal Saline Flushes

Recall Date: Friday, January 18th, 2008

Cardinal Health Statement on Alaris Pump Module Worldwide Voluntary Recall

Recall Date: Thursday, December 20th, 2007

AM2 PAT, Inc. Issues Nationwide Recall of Pre-Filled Heparin Lock Flush Solution USP (5 mL in 12 mL Syringes)

Recall Date: Thursday, December 20th, 2007

B. Braun Medical Inc. Issues Nationwide Recall of Normal Saline Flush Syringes with Lot Numbers Ending in SFR

Recall Date: Friday, September 14th, 2007

Urgent: Abbott Notifies Users of Precision Xtra™, Optium™, ReliOn® Ultima, Rite Aid® and Kroger® Blood Glucose Meters to Check Display Screens

Recall Date: Friday, August 31st, 2007

Firm Recall/State Recall

Recall Date: Tuesday, August 7th, 2007

Ortho-Clinical Diagnostics, Inc. Issues Voluntary, Nationwide Recall for Cardiac Marker

Recall Date: Friday, May 4th, 2007

ResMed Issues a Voluntary Recall for Certain S8 Flow Generators

Recall Date: Monday, April 23rd, 2007

Smith & Nephew Issues Nationwide Recall of RF Denervation Probes Used for the Spine

Recall Date: Monday, March 26th, 2007

Defibtech Announces a Worldwide Voluntary Recall of Lifeline and ReviveR Automated External Defibrillators

Recall Date: Tuesday, March 6th, 2007

Boston Scientific Announces Nationwide Recall of 51 Mach 1 Guide Catheters

Recall Date: Friday, December 15th, 2006

Rockline Announces Voluntary Product Withdrawal of Wet Wipes Products

Recall Date: Friday, November 17th, 2006

Endologix Announces Limited Voluntary Recall Of Visiflex 155 Mm Delivery Catheters

Recall Date: Thursday, November 9th, 2006

Roche Diagnostics Announces Nationwide Recall on Medical Device Used to Determine Blood Clotting Time

Recall Date: Thursday, October 19th, 2006

Gerber Products Company Issues Nationwide Allergy Alert on Undeclared Latex in Fashion Tint 9 Ounce Bottles (3 Packs)

Recall Date: Thursday, August 24th, 2006

Disetronic Medical Systems Inc Announces a Voluntary Nationwide Recall of Disetronic D-TRONplus Power Packs used in D-TRONplus Insulin Pumps

Recall Date: Thursday, July 13th, 2006

Firm Recall/State Recall

Recall Date: Friday, July 7th, 2006

Boston Scientific Announces Physician Communication Related to Products in Its CRM Group

Recall Date: Monday, June 26th, 2006

Sage Products Inc. Issues a Voluntary Recall of Comfort Shield® Perineal Care Washcloths in the U.S. and Canada

Recall Date: Friday, June 23rd, 2006

MRL, Inc. a Welch Allyn Company, Issues a Voluntary Worldwide Recall of Selected AED20 Automatic External Defibrillators

Recall Date: Thursday, June 15th, 2006

Hamilton Medical Issues a Medical Device Safety Alert on certain RAPHAEL Ventilators

Recall Date: Tuesday, June 6th, 2006

Respironics Issues Worldwide Recall of PLV® Continuum™ Ventilator

Recall Date: Friday, May 5th, 2006

Boca Medical Products, Inc. Issues Nationwide Recall of Insulin Syringe Product

Recall Date: Thursday, April 13th, 2006

Blackstone Medical, Inc. Issues Voluntary Recall of ICON™ Modular Fixation System

Recall Date: Wednesday, April 12th, 2006

Disetronic Medical Systems, Inc. Announces a Voluntary Nationwide Recall of all ACCU-CHEK™ Ultraflex Infusion Sets

Recall Date: Monday, April 3rd, 2006

Ossur Announces Voluntary Recall of Certain Models of the Total Knee

Recall Date: Wednesday, March 29th, 2006

The First Years Announces Voluntary Recall of Liquid-Filled Teethers

Recall Date: Friday, January 27th, 2006

Vapotherm ISSUES URGENT NATIONWIDE RECALL OF All Vapotherm® 2000i Respiratory Gas Humidification Devices

Recall Date: Tuesday, January 24th, 2006

Roche Diagnostics Issues a Worldwide Voluntary Recall of Some of its ACCU-CHEK® Aviva Meters

Recall Date: Monday, January 16th, 2006

Endologix Announces Limited Voluntary Recall of Powerlink System Delivery Catheter

Recall Date: Wednesday, December 14th, 2005

FDA Class I Classification Given to Baxter’s September 2005 Urgent Product Recall for Meridian Hemodialysis Instrument

Recall Date: Tuesday, December 13th, 2005

Boston Scientific Announces Worldwide Recall of Stainless Steel Greenfield® Vena Cava Filters Manufactured Before March 10, 2004

Recall Date: Friday, December 2nd, 2005

Omron 3-Way Instant Thermometers Recalled for Possible Safety Risk

Recall Date: Monday, October 24th, 2005

BioMerieux Issues Worldwide Correction Recall of VeriCal® Calibrator Set

Recall Date: Thursday, October 6th, 2005

Gambro Dasco S.p.A. Issues Worldwide Safety Alert for the Prisma System

Recall Date: Tuesday, August 16th, 2005

Disetronic Medical Systems, Inc. Announces a Voluntary Recall of the D-TRON Adapters, Used With the D-TRONplus Insulin Pump

Recall Date: Friday, July 29th, 2005

Guidant Initiates Worldwide Physician Communications Regarding Important Safety Information and Corrective Action about Certain Pacemakers

Recall Date: Monday, July 18th, 2005

Boston Scientific Announces Worldwide Recall of Hemashield® VantageT Peripheral Vascular Grafts

Recall Date: Monday, June 27th, 2005

Guidant Initiates Worldwide Physician Communications Regarding Important Safety Information and Corrective Action about Implantable Cardiac Defibrillators

Recall Date: Friday, June 24th, 2005

Qualitest Pharmaceuticals, Inc. Issues a Voluntary Nationwide Recall of Accusure Insulin Syringes 1cc 28 Gauge 1/2 Inch 100's

Recall Date: Tuesday, June 14th, 2005

MRL, Inc. a Welch Allyn Company Issues a Voluntary Worldwide Recall of Selected AED20 Automatic External Defibrillators

Recall Date: Tuesday, May 10th, 2005

Medtronic Announces Additional Devices Affected in Voluntary Recall of Certain Monophasic LifePak ® 500 Automated External Defibrillators

Recall Date: Friday, April 22nd, 2005

Kingswood Laboratories, Inc. Issues Nationwide Recall of Moi-Stir Oral Swabsticks

Recall Date: Friday, April 22nd, 2005

106 total items found
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