Short Fill: These products are being recalled because there is potential that vials with low fill volume were released into distribution.
Short Fill: These products are being recalled because there is potential that vials with low fill volume were released into distribution.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Ben Venue Laboratories Inc to request your refund or repair — edit it as you like.
Subject: Recall D-1377-2012 — Ben Venue Laboratories Inc Ben Venue Laboratories Inc recalls Octreotide Acetate Injection, 50 mcg/ Hello, I own a Ben Venue Laboratories Inc recalls Octreotide Acetate Injection, 50 mcg/mL (0.05 mg/mL), 1 mL single dose vials, packaged in 10 x 1 mL single dose vials that is covered by recall D-1377-2012 from Ben Venue Laboratories Inc. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
