Nipro GlucoPro Insulin Syringes: Recall - Needles may become detached and remain in the skin

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Title: Nipro GlucoPro Insulin Syringes: Recall - Needles may become detached and remain in the skin
MedWatch logo MedWatch - The FDA Safety Information and Adverse Event Reporting Program

Nipro GlucoPro Insulin Syringes: Recall

Audience: Pharmacists, diabetes healthcare professionals, consumers 

Nipro Medical Corporation and FDA notified healthcare professionals of a voluntary nationwide recall of all GlucoPro Insulin Syringes. These syringes may have needles that detach from the syringe. If the needle becomes detached from the syringe during use, it can become stuck in the insulin vial, push back into the syringe, or remain in the skin after injection. This recall includes all product codes and lot numbers with expiration dates before 2011-11 (November 1, 2011). Product was distributed nationwide, including Puerto Rico. Consumers who have GlucoPro Insulin Syringes should stop using and return them to point of sale for reimbursement.

Read the complete MedWatch 2010 Safety summary, including a link to the firm press release, at:

http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm198445.htm

 

 

 

    

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