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Eye Injection Kit Recall: Bausch + Lomb/Synergetics Inc. Removes Certain I-Pack Injection Kits Due to Potential Non-Sterility
Bausch + Lomb and its subsidiary, Synergetics, Inc. is recalling certain lots of I-Pack Injection Kits after being unable to verify that the products were fully sterilized. This recall involves removing devices from where they are used or sold.
The U.S. Food and Drug Administration (FDA) has identified this as a Class I recall, the most serious type of recall. This recall involves removing certain devices from where they are used or sold. If this device continues to be used, it may cause serious injuries, serious health consequences, or death.
Questions?
Customers in the U.S. with questions about this recall should contact their Bausch + Lomb sales representative or the customer service team at (800-338-2020).
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