Recall of Ultilet Insulin Syringe 30g 1/2cc

April 19, 2006 - Boca Medical Products and the FDA notified consumers and healthcare professionals of a recall of Ultilet Insulin Syringe 30g 1/2cc (Lot # - 5GEXI, NDC # - 08326-3002-50) because of possible bacterial presence of Bacillus Cereus and Staphylococcus Intermedius. This presents a risk of local infection due to soft tissue injection with a contaminated syringe as well a risk of introduction of contaminating organisms into a previously sterile vial. The introduced contamination may degrade the insulin, which could lead to problems maintaining insulin levels. This product has been distributed to the following states: FL, NY, MA, AL, SC, NC, CO, TX, MI, AR.

For any question related to the case consumers should call 1-800-354-8460. As always, pharmacies and members can contact the RxAmerica Customer Service Desk at 1-800-770-8014 if they have any questions about this product recall.