Epinephrine-Lidocaine HCl recall: Subpotent
Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use Intraocular injection Preservative Free NDC 71384-640-01 Not for resale. Office use…
Why was Epinephrine-Lidocaine HCl recalled?
Subpotent: Failing Test Results for Epinephrine
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
23APR018
- Product
- Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use Intraocular injection Preservative Free NDC 71384-640-01 Not for resale. Office use…
- Recalling firm
- Imprimis NJOF, LLC
- Quantity
- 364 bags (1 mL filled in 2 mL glass amber vials; 20 vials shipped in a bag)
- Distribution
- Nationwide
- Recall date
- October 11, 2023
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)