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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug

Wellness Pharmacy, Inc.: 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.; 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.

Agency Publication Date: September 12, 2013
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Affected Products

Product: Dexpanthenol 250mg/ml PF, Qty: 1mL, WELLNESS PHARMACY, 1-800-227-2627

Lot# 130605@52, Exp. 12/2/2013

Lot Numbers:
130605
Product: Magnesium Sulfate Hepta 50% PF, Single Use Vial, a) 2 mL, b) 10 mL, WELLNESS PHARMACY, 1-800-227-2627

Lot# 130613@38, Use By: 12/10/2013

Lot Numbers:
130613
Product: Methyl B12 1 mg/mL P.F., Single-Use Vial, a) 1 mL, b) 10 mL, WELLNESS PHARMACY, 1-800-227-2627

Lot# 130612@49, Use By: 12/9/2013

Lot Numbers:
130612
Product: NA. Phenylbutyrate 200 mg/mL, SDV, a) 10 mL, b) 25 mL, and c) 50 mL, WELLNESS PHARMACY, 1-800-227-2627

Lot# 130621@28, Use by: 10/19/2013

Lot Numbers:
130621
Product: RL Glutathione 100 mg/mL, SDV PF,a) 1 mL, b) 2 mL, c) 3 mL, and d) 4 mL, WELLNESS PHARMACY, 1-800-227-2627

Lot# 130710@27, Use By: 1/6/2014

Lot Numbers:
130710
Product: Dexpanthenol 250 mg/mL PF, Single Use Vial, 1 mL, WELLNESS PHARMACY, 1-800-227-2627

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

Lot Numbers:
130605

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 66188
Status: Resolved
Manufacturer: Wellness Pharmacy, Inc.
Manufactured In: United States
Units Affected: 6 products (1355 units; 590 Vials; 2687 Vials; 200 Vials; 34 Vials; 1355 Vials)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.