Ben Venue Laboratories Inc: 6 recalls on record

Recalls filed with 1 agency: FDA (6).

First recall on record: June 20, 2012. Most recent: August 27, 2014.

Risk classification: Class I: 2 · Class II: 4

Most recent recalls

DateAgencyProduct
August 27, 2014FDACYTARAbine for Injection USP, lyophiled in glass vials, 1 gram per vial, Rx only, Distrib…D-1543-2014
May 28, 2014FDAAcetylcysteine Solution, USP, 10%, 30 mL vial, Rx only, Ben Venue Laboratories, Inc., Bed…D-1326-2014
November 7, 2012FDALeucovorin Calcium Injection USP, single use vials, 10mg/mL; 50mL, Rx only, Manufactured …D-036-2013
October 3, 2012FDAVecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyop…D-1697-2012
June 20, 2012FDAOctreotide Acetate Injection, 50 mcg/mL (0.05 mg/mL), 1 mL single dose vials, packaged in…D-1377-2012
June 20, 2012FDAMidazolam HCl Injection, 5 mg/mL, 1 mL single use vials, packaged in 10 x 1 mL single use…D-1376-2012

Questions about this company

How many recalls does Ben Venue Laboratories Inc have?
Recalert has 6 U.S. recalls on record for Ben Venue Laboratories Inc, published between June 20, 2012 and August 27, 2014.
What was the most recent Ben Venue Laboratories Inc recall?
FDA recall D-1543-2014, published August 27, 2014: CYTARAbine for Injection USP, lyophiled in glass vials, 1 gram per vial, Rx only, Distributed by Bedford Laboratories, Bedford, OH 44146, Manufactured by Ben Venue Labs, Inc., Bedford, OH 44146, NDC …
Which agencies have handled Ben Venue Laboratories Inc recalls?
Ben Venue Laboratories Inc appears as the recalling firm in recalls from: FDA (6).

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