Drug Enforcement D-113-2013

Lack of Assurance of Sterility

Status

Terminated

Classification

Class II

Report Date

January 9, 2013

Termination Date

October 7, 2016

Product Information

Product description
Betamethasone Sodium Phosphate 6 mg/mL P Injection, Betamethasone Sodium Phosphate 6 mg/mL PF Injection, Betamethasone Sodium Phosphate 8 mg/mL PF Injection, Betamethasone Sodium Phosphate 12 mg/mL PF Injection, manufactured by New England Compounding Center, Framingham, MA
Product quantity
N/A
Reason for recall
Lack of Assurance of Sterility
Recall initiation reason
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Distribution pattern
Nationwide

Location & Firm

Recalling firm
New England Compounding Center
Address
697 Waverly St, N/A

United States
Voluntary / Mandated
Voluntary: Firm initiated
Status date

Codes & Dates

Recall number
D-113-2013
Event ID
63305
Recall initiation date
September 26, 2012
Center classification date
December 31, 2012
Code info
All lot codes
More code info