FDAFDA · Food and drugs·Recall number D-1377-2012
Octreotide Acetate Injection, 50 mcg/mL (0.05 mg/mL), 1 mL single dose vials, packaged in 10 x 1 mL single dose vials per pack, Rx only, Manufactured for: Bedford Laboratories, Bedford, OH 44146; Manufactured by: Ben Venue Laboratories, Inc., Bedford, OH 44146; NDC 55390-160-10; UPC 3 55390-160-10 1.
Published June 20, 2012 · Recall initiated: May 1, 2012
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Short Fill: These products are being recalled because there is potential that vials with low fill volume were released into distribution.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Ben Venue Laboratories Inc
- Distributor
- Nationwide and Puerto Rico.
- Lot
- Lot # 2006500, Exp 08/31/12
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States