Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Epinephrine/Lidocaine HCl Recalled by Edge Pharma, LLC Due to Labeling: Incorrect or Missing Lot and/or Exp Date
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Edge Pharma, LLC directly.
Affected Products
Epinephrine/Lidocaine HCl, Sterile Ophthalmic Solution for Injection, 0.8 mL per syringe, Single Use Syringe, 0.025%/0.75%, Rx only, Edge Pharma LLC 856 Hercules Dr. Colchester, VT 05446, NDC 05446-0863-01
Quantity: 60 syringes
Why Was This Recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date
Where Was This Sold?
This product was distributed to 1 state: PA
About Edge Pharma, LLC
Edge Pharma, LLC has 62 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report