Lidocaine HCL/ Sodium Bicarb, 1%/0.5% 0.5 mL SYR PF, packaged in a 3 cc pre-filled syringe, Rx only
Reason Non-Sterility: failed sterility test result.
Yes — there is an active recall. 60 ongoing FDA recalls mention Lidocaine (365 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Lidocaine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Reason Non-Sterility: failed sterility test result.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility; all compounded products within expiry produced using recalled filters
Reason Lack of Assurance of Sterility
Reason Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a voluntary field action for the Methylprednisolone Acetate/Lidocaine HCl…
Reason Failed Stability Specifications: The recalled lots did not meet the specification for color and pH throughout shelf life.
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Lack of Processing Controls
Reason Lack of Processing Controls
Reason Lack of Processing Controls
Reason Lack of Assurance of Sterility
Reason Lack of Assurance of Sterility
Reason Marketed without an approved NDA/ANDA
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