FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

Medaus NA Ascorbate 500 mg/mL Recall

NA Ascorbate 500 mg/mL, non corn PF, 100ML, Medaus Pharmacy, 1-800-526-9183

Medaus, Inc. · Birmingham, AL

Risk level
Class II
Reported by FDA
Sep 25, 2013
Recall ID
D-1055-2013
Check your lot numberHow we source this data

Summary

Medaus recalled NA Ascorbate 500 mg/mL starting Aug 23, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1055-2013 on Sep 25, 2013. Reason: Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured. Status: Terminated.

Why it was recalled

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

Product description

NA Ascorbate 500 mg/mL, non corn PF, 100ML, Medaus Pharmacy, 1-800-526-9183

Lot numbers, UPCs & expiration codes

LOT # 130613-8, Exp 12/10/2013

Where it was sold

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-1055-2013
Classification
Class II
Status
Terminated
Recall initiated
Aug 23, 2013
FDA report date
Sep 25, 2013
Quantity
8750 mL
Recall type
Voluntary: Firm initiated
Recalling firm
Medaus, Inc.

Original FDA data

Every field from FDA enforcement report D-1055-2013, exactly as published.

Show all FDA fields
City
Birmingham
State
AL
Status
Terminated
Country
United States
Event ID
66172
Address
6801 Cahaba Valley Rd Ste 116
Code information
LOT # 130613-8, Exp 12/10/2013
Postal code
35242-9609
Report date
Sep 25, 2013
Product type
Drugs
Recall number
D-1055-2013
Classification
Class II
Recalling firm
Medaus, Inc.
Product quantity
8750 mL
Termination date
Jul 16, 2014
Reason for recall
Lack of Assurance of Sterility: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.
Voluntary / mandated
Voluntary: Firm initiated
Product description
NA Ascorbate 500 mg/mL, non corn PF, 100ML, Medaus Pharmacy, 1-800-526-9183
Distribution pattern
Nationwide
Recall initiation date
Aug 23, 2013
Initial firm notification
Telephone
Center classification date
Sep 13, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1055-2013, published Sep 25, 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

Other recent drug recalls