PlainRecalls
FDA Drug Critical Class I Terminated

Methylprednisolone Acetate (PF) 40 mg/ml Injection, supplied in 1 mL, 2 mL and 5 mL vials, manufactured by New England Compounding Center, Framingham, MA

Reported: January 9, 2013 Initiated: September 26, 2012 #D-109-2013

Product Description

Methylprednisolone Acetate (PF) 40 mg/ml Injection, supplied in 1 mL, 2 mL and 5 mL vials, manufactured by New England Compounding Center, Framingham, MA

Reason for Recall

Non-Sterility

Details

Units Affected
9062 vials
Distribution
Nationwide
Location
Framingham, MA

Frequently Asked Questions

What product was recalled?
Methylprednisolone Acetate (PF) 40 mg/ml Injection, supplied in 1 mL, 2 mL and 5 mL vials, manufactured by New England Compounding Center, Framingham, MA. Recalled by New England Compounding Center. Units affected: 9062 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-109-2013.