Reported Jun 20, 2012 · Terminated

Octreotide Acetate Injection, 50 mcg/mL (0.05 mg/mL), 1 mL single dose vials, packaged in 10 x 1 mL single dose vials…

Ben Venue Laboratories Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Ben Venue Laboratories Inc · 300 Northfield Rd · Bedford, OH · 44146

Is this the product you have?

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

4 of 4 products

Products covered by this recall
#Product as published
1Bedford Laboratories, Bedford, OH 44146
2Manufactured by: Ben Venue Laboratories, Inc., Bedford, OH 44146
3NDC 55390-160-10
4UPC 3 55390-160-10 1.
Lot codes and dates
    • Lot # 2006500
    • Exp 08/31/12
Amount recalled
6,515 packs

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Short Fill: These products are being recalled because there is potential that vials with low fill volume were released into distribution.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Aug 21, 2013 · Data as of Sep 19, 5:46 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.