PlainRecalls
FDA Drug Moderate Class II Terminated

Betamethasone Repository 6 mg/mL PF Injection and Betamethasone Repository 6 mg/mL P Injection, manufactured by New England Compounding Center, Framingham, MA

Reported: January 9, 2013 Initiated: September 26, 2012 #D-112-2013

Product Description

Betamethasone Repository 6 mg/mL PF Injection and Betamethasone Repository 6 mg/mL P Injection, manufactured by New England Compounding Center, Framingham, MA

Reason for Recall

Lack of Assurance of Sterility

Details

Units Affected
N/A
Distribution
Nationwide
Location
Framingham, MA

Frequently Asked Questions

What product was recalled?
Betamethasone Repository 6 mg/mL PF Injection and Betamethasone Repository 6 mg/mL P Injection, manufactured by New England Compounding Center, Framingham, MA. Recalled by New England Compounding Center. Units affected: N/A.
Why was this product recalled?
Lack of Assurance of Sterility
Which agency issued this recall?
This recall was issued by the FDA Drug on January 9, 2013. Severity: Moderate. Recall number: D-112-2013.