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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
May 24, 2017
Recall ID
D-0788-2017
Check your lot numberHow we source this data

Summary

Baxter Healthcare recalled Fluconazole Injection starting May 15, 2017. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0788-2017 on May 24, 2017. Reason: Lack of assurance of sterility: customer complaints received for the presence of leaks. Status: Terminated.

Why it was recalled

Lack of assurance of sterility: customer complaints received for the presence of leaks.

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/P344028A, Exp 12/31/17; P352377, Exp 8/31/18; P348136, Exp 4/30/18

Where it was sold

US and foreign countries: United Arab Emirates, Colombia, and Canada

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-0788-2017
Classification
Class II
Status
Terminated
Recall initiated
May 15, 2017
FDA report date
May 24, 2017
Quantity
113,590 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Baxter Healthcare Corporation

Original FDA data

Every field from FDA enforcement report D-0788-2017, exactly as published.

Show all FDA fields
City
Deerfield
State
IL
Status
Terminated
Country
United States
Event ID
77247
Address
1 Baxter Pkwy
Code information
Lot #: P344028/P344028A, Exp 12/31/17; P352377, Exp 8/31/18; P348136, Exp 4/30/18
Postal code
60015-4625
Report date
May 24, 2017
Product type
Drugs
Recall number
D-0788-2017
Classification
Class II
Recalling firm
Baxter Healthcare Corporation
Product quantity
113,590 bags
Termination date
Aug 10, 2018
Reason for recall
Lack of assurance of sterility: customer complaints received for the presence of leaks.
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
US and foreign countries: United Arab Emirates, Colombia, and Canada
Recall initiation date
May 15, 2017
Center classification date
May 18, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0788-2017, published May 24, 2017. 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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