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FDA Drug Recall

Rick

Updated: May 20, 2021

As of May 5, 2021, Hospira has issued a recall of specific lots of 0.5% Bupivacaine Hydrochloride and Lidocaine HCL. If you have either lot EG6023 of 0.5% Bupivacaine Hydrochloride Injection, USP 0.5% 30 mL or lot EG8933 of Lidocaine HCl Injection USP, 1% 30 mL, it should be removed from stock immediately and the manufacturer (or the dealer through whom it was purchased) should be contacted. Hospira has identified mislabeling whereby a portion of each lot was incorrectly labeled as the other product. This issue was identified as part of the investigation of a confirmed customer report.


For further information, contact Hospira, or see the full report from the FDA.




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The information contained herein is for educational purposes and for the benefit of licensed health care professionals. Much equipment in the dental office is under high pressure, carries high voltage electricity and/or can generate extreme temperatures.  Care should always be taken when performing repairs or maintenance. Under normal circumstances, equipment should be turned off, depressurized, and disconnected from power before performing service. It is the responsibility of the end-user to recognize and exercise appropriate caution.  All content copyright Dental-Techguru LLC.

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