Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL recall
Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free, 1 mL Single-Use vials, Rx only, Imprimis NJOF, LLC 1705 Route 46 West, Unit 6B…
Why was Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL recalled?
Out of specification for assay
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
Lot #: 23JUL028, Exp. Date 8/1/2024; 23AUG053, Exp. Date 8/30/2024
- Product
- Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free, 1 mL Single-Use vials, Rx only, Imprimis NJOF, LLC 1705 Route 46 West, Unit 6B…
- Recalling firm
- Imprimis NJOF, LLC
- Quantity
- 15,414 units
- Distribution
- Nationwide within the United States
- Recall date
- May 8, 2024
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (drug)