Epinephrine/Lidocaine HCl — Class III drug recall D-0307-2021
Terminated recall by Edge Pharma, LLC, reported 2021-03-24. Labeling: Incorrect or Missing Lot and/or Exp Date
| Recall number | D-0307-2021 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Edge Pharma, LLC, Colchester, VT, United States |
| Recall initiated | 2020-12-22 |
| Classified | 2021-03-18 |
| Reported by FDA | 2021-03-24 |
| Terminated | 2021-06-10 |
| Quantity | 60 syringes |
| Reason classes | labeling |
| NDC | 05446-0863-01 |
| Expiration dates | 2020-12-03 |
Product
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
Reason for recall
Labeling: Incorrect or Missing Lot and/or Exp Date
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0307-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.