PlainRecalls
FDA Drug Moderate Class II Terminated

Sevoflurane, USP (Inhalation Anesthetic), Rx Only, 250 mL Amber Bottle. Manufactured By: Piramal Critical Care, 3950 Schelden Circle, Bethlehem, PA 18017. NDC: 66794-015-25.

Reported: May 7, 2014 Initiated: April 7, 2014 #D-1262-2014

Product Description

Sevoflurane, USP (Inhalation Anesthetic), Rx Only, 250 mL Amber Bottle. Manufactured By: Piramal Critical Care, 3950 Schelden Circle, Bethlehem, PA 18017. NDC: 66794-015-25.

Reason for Recall

Failed pH Specifications: product was too acidic.

Details

Units Affected
12,600 bottles
Distribution
To wholesale distributors and retailers located Nationwide.
Location
Bethlehem, PA

Frequently Asked Questions

What product was recalled?
Sevoflurane, USP (Inhalation Anesthetic), Rx Only, 250 mL Amber Bottle. Manufactured By: Piramal Critical Care, 3950 Schelden Circle, Bethlehem, PA 18017. NDC: 66794-015-25.. Recalled by Piramal Critical Care, Inc.. Units affected: 12,600 bottles.
Why was this product recalled?
Failed pH Specifications: product was too acidic.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 7, 2014. Severity: Moderate. Recall number: D-1262-2014.