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GlucoPro insulin syringes recalled for faulty needles
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Nipro Medical Corporation has initiated a nationwide recall of GlucoPro insulin syringes because the defective products may contain needles that can detach from the syringe.
If the needle becomes detached from the syringe, it may become stuck in the insulin vial, push back into the syringe or remain in the skin after injection.
All syringes with expiration dates before Nov. 1, 2011 are included in the recall. The product was distributed nationwide, including Puerto Rico.
No injuries have been reported related to use of the product.
The GlucoPro syringe used in combination with the Amigo Insulin pump is not included in this recall.
The FDA warned patients with diabetes, pharmacists and other health care professionals in possession of the recalled syringes to cease use and return them to the point of sale for reimbursement.
For a full list of all recalled product codes and lot numbers with expiration dates, visit the FDA website.
Adverse events or problems experienced with use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program.