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Class II: temporary or reversible health riskTerminated

Baxter Healthcare Fluconazole Injection Recall

Fluconazole Injection, USP, 200 mg/100 mL (2mg/mL), 100 mL Single-Dose Intravia Contain…

Baxter Healthcare Corporation · Deerfield, IL

Risk level
Class II
Reported by FDA
Dec 28, 2016
Recall ID
D-0206-2017
Check your lot numberHow we source this data

Summary

Baxter Healthcare recalled Fluconazole Injection starting Dec 6, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0206-2017 on Dec 28, 2016. Reason: Lack of Assurance of Sterility: confirmed customer complaints of leaking bags. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: confirmed customer complaints of leaking bags.

Product description

Fluconazole Injection, USP, 200 mg/100 mL (2mg/mL), 100 mL Single-Dose Intravia Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product Code 2J1446, NDC 0338-6046-48.

Lot numbers, UPCs & expiration codes

Lot #: P344028 on bags, P344028A on shipping container, Exp 12/31/2017

Where it was sold

United States, United Arab Emirates, and Colombia

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-0206-2017
Classification
Class II
Status
Terminated
Recall initiated
Dec 6, 2016
FDA report date
Dec 28, 2016
Quantity
30,910 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Baxter Healthcare Corporation

Original FDA data

Every field from FDA enforcement report D-0206-2017, exactly as published.

Show all FDA fields
City
Deerfield
State
IL
Status
Terminated
Country
United States
Event ID
75831
Address
1 Baxter Pkwy
Code information
Lot #: P344028 on bags, P344028A on shipping container, Exp 12/31/2017
Postal code
60015-4625
Report date
Dec 28, 2016
Product type
Drugs
Recall number
D-0206-2017
Classification
Class II
Recalling firm
Baxter Healthcare Corporation
Product quantity
30,910 bags
Termination date
Feb 12, 2018
Reason for recall
Lack of Assurance of Sterility: confirmed customer complaints of leaking bags.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Fluconazole Injection, USP, 200 mg/100 mL (2mg/mL), 100 mL Single-Dose Intravia Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product Code 2J1446, NDC 0338-6046-48.
Distribution pattern
United States, United Arab Emirates, and Colombia
Recall initiation date
Dec 6, 2016
Initial firm notification
Letter
Center classification date
Dec 19, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0206-2017, published Dec 28, 2016. 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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