Epinephrine liquid 1:1000 recall: Sterility Concern
Epinephrine liquid 1:1000, RX, glass vial
Why was Epinephrine liquid 1:1000 recalled?
Lack of sterility assurance.
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?
10102018@13 exp 1/8/19, 10222018@33 exp 1/20/19,
- Product
- Epinephrine liquid 1:1000, RX, glass vial
- Recalling firm
- Hiers Enterprises, LLC dba Northwest Compounding Pharmacy
- Quantity
- 50 ml
- Distribution
- Product was distributed exclusively in the state of Oregon to 3 Medical facilities, 1 Physician's office and 80 consumers/patients. These are compounded products - labels vary for each compound - specific to each patient. Firm did not provide labeling.
- Recall date
- January 9, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)