US Recall News » FDA Press Releases

The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex That May Contain Particulate Matter

FDA — Thu, 18 Mar 2010 00:00:00 +0000

Stay up to date on: product recalls.The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex That May Contain Particulate Matter

Stay up to date on: product recalls.

The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex That May Contain Particulate Matter

Teleflex Incorporated Announces Worldwide Voluntary Recall of Arrow Select IV Tubing Sets, Accessories, and Certain Embolectomy Catheters

FDA — Tue, 16 Mar 2010 00:00:00 +0000

Stay up to date on: product recalls.Teleflex Incorporated Announces Worldwide Voluntary Recall of Arrow Select IV Tubing Sets, Accessories, and Certain Embolectomy Catheters

Stay up to date on: product recalls.

Teleflex Incorporated Announces Worldwide Voluntary Recall of Arrow Select IV Tubing Sets, Accessories, and Certain Embolectomy Catheters

LifeScan Recalls 8 Lots of OneTouch, SureStep Test Strips Due To Inaccurate

FDA — Sat, 27 Feb 2010 00:00:00 +0000

LifeScan is recalling eight lots of OneTouch, SureStep Test Strips, used by people with diabetes to measure their blood glucose levels at home.

Stay up to date on: product recalls.

LifeScan Recalls 8 Lots of OneTouch, SureStep Test Strips Due To Inaccurate

Acacia Recalls IV Extension Sets with BD Q-Syte Luer Access Device

FDA — Wed, 10 Feb 2010 00:00:00 +0000

The IV Extension Set with BD Q-Syte Luer Access device is intended for use with other infusion therapy products in the administration of fluids into the intravenous system.

Stay up to date on: product recalls.

Acacia Recalls IV Extension Sets with BD Q-Syte Luer Access Device

Cardiac Science Notifies AED Customers of Medical Device Recall

FDA — Wed, 10 Feb 2010 00:00:00 +0000

Cardiac Science detected this issue through its internal quality systems and has received no complaints or reports of this problem in the field.

Stay up to date on: product recalls.

Cardiac Science Notifies AED Customers of Medical Device Recall

BD Announces Worldwide Voluntary Recall ofBD Q-Sytea Luer Access Devices and BD Nexiva Closed IV Catheter Systems

FDA — Wed, 10 Feb 2010 00:00:00 +0000

The BD Nexiva product has two BD Q-Syte devices within the package that could potentially be subject to the manufacturing deviation previously referenced.

Stay up to date on: product recalls.

BD Announces Worldwide Voluntary Recall ofBD Q-Sytea Luer Access Devices and BD Nexiva Closed IV Catheter Systems

Edwards Lifesciences Aquarius Hemodialysis System

FDA — Fri, 29 Jan 2010 00:00:00 +0000

Edwards Lifesciences has announced a Class I recall of the Aquarius Hemodialysis System due to reports of clinically significant fluid imbalance and the potential for users to repeatedly override the fluid imbalance alarm.

Stay up to date on: product recalls.

Edwards Lifesciences Aquarius Hemodialysis System

Hettich Centrifuges with 2050 and 2076 Plastic Rotors

FDA — Fri, 29 Jan 2010 00:00:00 +0000

A Class I recall of Hettich Centrifuges with 2050 and 2076 plastic rotors, used in combination with the Mikro 12-24, Mikro 20, Haematokrit 20 and Haematokrit 24 bench top plastic centrifuges.

Stay up to date on: product recalls.

Hettich Centrifuges with 2050 and 2076 Plastic Rotors

Recalled Infusion Set Needles Manufactured by Nipro for Exelint

FDA — Fri, 29 Jan 2010 00:00:00 +0000

These needles should be designed to penetrate the port without cutting and dislodging any silicone cores from the ports into which they are inserted.

Stay up to date on: product recalls.

Recalled Infusion Set Needles Manufactured by Nipro for Exelint

FDA Recalls Exel/Exelint Huber Needles

FDA — Thu, 28 Jan 2010 00:00:00 +0000

There are more than 2 million units impacted by this recall in distribution nationwide. Recalled needles were manufactured from January 2007 to August 2009.

Stay up to date on: product recalls.

FDA Recalls Exel/Exelint Huber Needles

Hettich Centrifuges Recalls Plastic Hematocrit Rotors: Injury Risk

FDA — Sat, 23 Jan 2010 00:00:00 +0000

Hettich Centrifuges recalls of 2050 and 2076 plastic hematocrit rotors in combination with the Mikro 12-24, Mikro 20, Haematokrit 20 and Haematokrit 24 bench top plastic centrifuges.

Stay up to date on: product recalls.

Hettich Centrifuges Recalls Plastic Hematocrit Rotors: Injury Risk

Nipro Medical Recalls GlucoPro Insulin Syringes

FDA — Sat, 23 Jan 2010 00:00:00 +0000

Nipro Medical recalls GlucoPro Insulin Syringes because these syringes may have needles that detach from the syringe.

Stay up to date on: product recalls.

Nipro Medical Recalls GlucoPro Insulin Syringes

MuscleMaster.com Recalls Certain BodyBuilding Products

FDA — Sat, 16 Jan 2010 00:00:00 +0000

FDA informed MuscleMaster.com that it believes that the Recalled Products contain ingredients that are steroids.

Stay up to date on: product recalls.

MuscleMaster.com Recalls Certain BodyBuilding Products

McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products

FDA — Sat, 16 Jan 2010 00:00:00 +0000

Please see our post from yesterday regarding this OTC medication recall by McNeil Consumer Healthcare.

Stay up to date on: product recalls.

McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products

ev3 Endovascular Inc. Trailblazer Support Catheter: Class I Recall

FDA — Thu, 07 Jan 2010 00:00:00 +0000

Class 1 recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death.

Stay up to date on: product recalls.

ev3 Endovascular Inc. Trailblazer Support Catheter: Class I Recall

Nationwide Recall Of All Lots Of Tylenol Arthritis Pain 100 Count With Ez-Open Cap

FDA — Tue, 29 Dec 2009 00:00:00 +0000

Consumers who purchased TYLENOL ® Arthritis Pain Caplet 100 count bottles with the distinctive red EZ-OPEN CAP from the lots included in this recall should stop using the product and contact McNeil for instructions on a refund or replacement.

Stay up to date on: product recalls.

Nationwide Recall Of All Lots Of Tylenol Arthritis Pain 100 Count With Ez-Open Cap

Encompass Group Recalls Thermoflect Product Line

FDA — Tue, 29 Dec 2009 00:00:00 +0000

Encompass Group Corporate recalls Thermoflect product line for relabeling regarding its use in the MR (Magnetic Resonance) environment.

Stay up to date on: product recalls.

Encompass Group Recalls Thermoflect Product Line

Teva Animal Health, Inc. Expands Recall of Ketamine Hydrochloride Injection, USP CIII 100mg/mL in 10mL vials

FDA — Tue, 22 Dec 2009 00:00:00 +0000

Veterinarians who have this product in their possession are instructed to cease using the product immediately and return it to their distributor.

Stay up to date on: product recalls.

Teva Animal Health, Inc. Expands Recall of Ketamine Hydrochloride Injection, USP CIII 100mg/mL in 10mL vials

The Medicines Company Recalls Certain Lots of Cleviprex: Particulate Matter

FDA — Thu, 17 Dec 2009 00:00:00 +0000

The Medicines Company recalls 11 lots of Cleviprex ® (clevidipine butyrate) injectable emulsion due to the potential presence of visible particulate matter.

Stay up to date on: product recalls.

The Medicines Company Recalls Certain Lots of Cleviprex: Particulate Matter

Atlas Operations Recalls Specific Lots of Sexual Enhancement Products Marketed as Dietary Supplements

FDA — Tue, 15 Dec 2009 00:00:00 +0000

Erectile Dysfunction is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance.

Stay up to date on: product recalls.

Atlas Operations Recalls Specific Lots of Sexual Enhancement Products Marketed as Dietary Supplements