Accusure Insulin Syringe Recall: Needle May Detach from the Syringe

Two lots of Accusure insulin syringes have been recalled due to defective needles that can detach from the syringes during use, according to a notice posted by the FDA on Friday.

The Accusure insulin syringe recall was issued after the manufacturer, Qualtest Pharmaceuticals, Inc., received at least three reports of needles on the short needle syringes breaking off. If the needle detaches, it can slide back into the syringe during use, remain in the skin after injection or become stuck in the insulin vial.

The recall includes Accusure Insulin Syringes (1/2 cc โ€“ 31 G โ€“ Short Needle) with lot number 7CPT1 (Expiration 03/2012) โ€“ NDC 0603-7002-21. These needles were distributed between May 2007 and June 2008. The recall also includes Accusure Insulin Syringes (1/2 cc โ€“ 31 G โ€“ Short Needle) with lot number 6JCB1 (Expiration 10/2011) โ€“ NDC 0603-7001-21. The lot numbers can be found on the white paper backing on each syringe.

Spinal-Cord-Stimulation-Lawsuit
Spinal-Cord-Stimulation-Lawsuit

Anyone with syringes affected by the insulin syringe recall has been urged by the manufacturer to stop using them and to contact Qualitest at 1-800-444-4011 for replacements. However, product liability lawyers recommend that any consumers who have suffered a severe physical injury requiring medical treatment as a result of the defective insulin syringes, should preserve any remaining syringes in a manner to prevent further use until it has been determined whether an insulin syring recall lawsuit will be pursued.


0 Comments


This field is for validation purposes and should be left unchanged.

Share Your Comments

This field is hidden when viewing the form
I authorize the above comments be posted on this page
Post Comment
Weekly Digest Opt-In

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

MORE TOP STORIES

Pfizer continues to face Depo-Provera lawsuits from across the U.S., including one by a woman who says she learned of her brain tumor nearly 30 years after she stopped receiving the injections.
A Mounjaro vision loss lawsuit accuses Eli Lilly of failing to properly investigate the drug’s side effects and provide proper warnings before marketing it to the public.
According to a recently filed lawsuit, exposure to Suboxone oral film strips caused an Illinois man to suffer severe tooth decay that required extensive dental work.