Key Takeaway

Epinephrine liquid 1:1000, RX, glass vial by Hiers Enterprises, LLC dba Northwest Compounding Pharmacy was recalled on January 2, 2019. The hazard: Lack of sterility assurance.

FDA Drug Class II Terminated

Epinephrine liquid 1:1000, RX, glass vial

Recalled: January 2, 2019 ~50 ml units affected D-0393-2019

Description

Epinephrine liquid 1:1000, RX, glass vial

Hazard / Reason

Lack of sterility assurance.

Class II: Product that may cause temporary or medically reversible health consequences.

Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.

Products Affected

Epinephrine liquid 1:1000, RX, glass vial

Drugs

Company Information

Hiers Enterprises, LLC dba Northwest Compounding Pharmacy

Roseburg, OR, United States

View all 17 recalls by Hiers Enterprises, LLC dba Northwest Compounding Pharmacy →

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.

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Frequently Asked Questions

Is this recall still active?

Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.

How do I check if my product is affected?

Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.

What remedy is available for this recall?

Check the remedy section above or contact the manufacturer directly for current remedy options.

Where can I find the original recall notice?

This recall was issued by FDA Drug. Visit the agency's official website for the original notice.

Data sourced from FDA Drug Enforcement. Recall information may not reflect the most current status. RecallDex is not affiliated with any US government agency. Contact the manufacturer or relevant agency for the latest information.