Edge Pharma, LLC recalls Epinephrine/Lidocaine HCl, Sterile Ophthalmic Solution for Injection, 0.8 mL per syringe, Single Use Syringe, 0.025%/0.…
- Recall date
- December 22, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0307-2021
- FDA classification
- Class III
- Brand / firm
- Edge Pharma, LLC
- Sold / distributed
- PA only
Why it was recalled
Labeling: Incorrect or Missing Lot and/or Exp Date
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
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
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