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Nipro GlucoPro Insulin Syringes with expiration dates before Nov. 1, 2011

Discussion in 'Product Recalls' started by Ellen, Jan 22, 2010.

  1. Ellen

    Ellen Senior Member

    Oct 22, 2005
    Nipro Medical Corp. of Miami is recalling all GlucoPro Insulin Syringes with expiration dates before Nov. 1, 2011, not including the GlucoPro syringe for use with the Amigo insulin pump, because the needles can detach. This defect could allow the needle to get stuck in the insulin vial, be pushed backed into the syringe or stay in the skin after injection. No injuries have been reported. The needles were available nationwide, including Puerto Rico. Details: by phone at 305-599-7174, extension 249.


    Nipro Medical Corporation Issues a Voluntary Recall of All GlucoPro Insulin Syringes

    Recall -- Firm Press Release

    FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
    Nipro Medical Corporation Issues a Voluntary Recall of All GlucoPro Insulin Syringes

    Jessica Oswald
    305.599.7174 x249
    (EST: 9 am – 5 pm)
    FOR IMMEDIATE RELEASE - January 21, 2010 - Nipro Medical Corporation, Miami FL, is initiating a nationwide recall of all GlucoPro Insulin Syringes (This does not include the GlucoPro syringe specific for use with the Amigo Insulin pump). 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.
    Consumers who have GlucoPro Insulin Syringes should stop using and return them to point of sale for reimbursement.
    This recall includes all product codes and lot numbers with expiration dates before 2011-11 (Nov 1, 2011).
    Product CodeLot #Expiry dateJD+01U3008-5CA080222011-11JD+01U3013-5CA080132011-06JD+01U3013-5CA080172011-08JD+01U3108-5CA080132011-06JD+01U3108-5CA080172011-08JD+03U3008-5CC080222011-11JD+03U3013-5CC080132011-06JD+03U3013-5CC080172011-08JD+03U3108-5CC080132011-06JD+03U3108-5CC080172011-08JD+05U3008-5CB080222011-11JD+05U3013-5CB080132011-06JD+05U3013-5CB080172011-08JD+05U3108-5CB080132011-06JD+05U3108-5CB080172011-08
    The firm voluntarily recalled the products after learning of the possibility of needle detachment. FDA has been apprised of this action.
    No injuries have been reported to date.
    Product was distributed nationwide, including Puerto Rico.
    Company is notifying its distributors and customers by Fax and Email and is arranging for return of all recalled products.
    Consumers with questions may contact the company at 305.599.7174 x249.
    Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.​
    Last edited: Jan 23, 2010

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