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Class II: temporary or reversible health riskTerminated

Athenex Pharma Solutions Epinephrine Injection 8 mg per 250 mL in 0 Recall

Epinephrine Injection 8 mg per 250 mL in 0

Athenex Pharma Solutions, LLC · Clarence, NY

Risk level
Class II
Reported by FDA
Mar 30, 2022
Recall ID
D-0712-2022
Check your lot numberHow we source this data

Summary

Athenex Pharma Solutions recalled Epinephrine Injection 8 mg per 250 mL in 0 starting Mar 14, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0712-2022 on Mar 30, 2022. Reason: Defective container. Status: Terminated.

Why it was recalled

Defective container

Product description

Epinephrine Injection 8 mg per 250 mL in 0.9% Sodium Chloride, 8mg, 250 mL excel bag, Rx only, Athenex Pharma Solutions, LLC, Clarence, NY, 14031, NDC 76154-814-15

Lot numbers, UPCs & expiration codes

Lot #: F2101780, F2101781, Exp 6/21/22

Where it was sold

USA nationwide.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0712-2022
Classification
Class II
Status
Terminated
Recall initiated
Mar 14, 2022
FDA report date
Mar 30, 2022
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
Athenex Pharma Solutions, LLC

Original FDA data

Every field from FDA enforcement report D-0712-2022, exactly as published.

Show all FDA fields
City
Clarence
State
NY
Status
Terminated
Country
United States
Event ID
89779
Address
11342 Main St
Code information
Lot #: F2101780, F2101781, Exp 6/21/22
Postal code
14031-1718
Report date
Mar 30, 2022
Product type
Drugs
Recall number
D-0712-2022
Classification
Class II
Recalling firm
Athenex Pharma Solutions, LLC
Termination date
Aug 4, 2022
Reason for recall
Defective container
Voluntary / mandated
Voluntary: Firm initiated
Product description
Epinephrine Injection 8 mg per 250 mL in 0.9% Sodium Chloride, 8mg, 250 mL excel bag, Rx only, Athenex Pharma Solutions, LLC, Clarence, NY, 14031, NDC 76154-814-15
Distribution pattern
USA nationwide.
Recall initiation date
Mar 14, 2022
Initial firm notification
Letter
Center classification date
Mar 21, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0712-2022, published Mar 30, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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