PlainRecalls
FDA Drug Critical Class I Terminated

Methylprednisolone Acetate 40 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

Reported: January 9, 2013 Initiated: September 26, 2012 #D-110-2013

Product Description

Methylprednisolone Acetate 40 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

Reason for Recall

Non-Sterility

Details

Units Affected
5130 vials
Distribution
Nationwide
Location
Framingham, MA

Frequently Asked Questions

What product was recalled?
Methylprednisolone Acetate 40 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA. Recalled by New England Compounding Center. Units affected: 5130 vials.
Why was this product recalled?
Non-Sterility
Which agency issued this recall?
This recall was issued by the FDA Drug on January 9, 2013. Severity: Critical. Recall number: D-110-2013.