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Class II: temporary or reversible health riskTerminated

Wellness Pharmacy Dexpanthenol 250 mg/mL PF Recall

Dexpanthenol 250 mg/mL PF, Single Use Vial, 1 mL, WELLNESS PHARMACY, 1-800-227-2627

Wellness Pharmacy, Inc. · Birmingham, AL

Risk level
Class II
Reported by FDA
Sep 18, 2013
Recall ID
D-1035-2013
Check your lot numberHow we source this data

Summary

Wellness Pharmacy recalled Dexpanthenol 250 mg/mL PF starting Aug 23, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1035-2013 on Sep 18, 2013. Reason: Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable.

Product description

Dexpanthenol 250 mg/mL PF, Single Use Vial, 1 mL, WELLNESS PHARMACY, 1-800-227-2627

Lot numbers, UPCs & expiration codes

Lot# 130605@52, Exp. 12/2/13

Where it was sold

Nationwide and Puerto Rico

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-1035-2013
Classification
Class II
Status
Terminated
Recall initiated
Aug 23, 2013
FDA report date
Sep 18, 2013
Quantity
1355 Vials
Recall type
Voluntary: Firm initiated
Recalling firm
Wellness Pharmacy, Inc.

Original FDA data

Every field from FDA enforcement report D-1035-2013, exactly as published.

Show all FDA fields
City
Birmingham
State
AL
Status
Terminated
Country
United States
Event ID
66188
Address
3401 Independence Drive Suite 231
Code information
Lot# 130605@52, Exp. 12/2/13
Postal code
35209-8326
Report date
Sep 18, 2013
Product type
Drugs
Recall number
D-1035-2013
Classification
Class II
Recalling firm
Wellness Pharmacy, Inc.
Product quantity
1355 Vials
Termination date
Jun 3, 2014
Reason for recall
Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Dexpanthenol 250 mg/mL PF, Single Use Vial, 1 mL, WELLNESS PHARMACY, 1-800-227-2627
Distribution pattern
Nationwide and Puerto Rico
Recall initiation date
Aug 23, 2013
Initial firm notification
Telephone
Center classification date
Sep 12, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1035-2013, published Sep 18, 2013. 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.

How we source and update recall data · Report incorrect information

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