Severity
Critical
FDA Drug recall · Reported October 3, 2012
Presence of Particulate Matter
Ben Venue Laboratories Inc recalled Vecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyop… - a critical-severity action.
Vecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyop… was recalled by Ben Venue Laboratories Inc in October 3, 2012. Reason: Presence of Particulate Matter. Check the official notice for the remedy. Verify recall #D-1697-2012 with the FDA Drug before acting.
The recall
Ben Venue Laboratories Inc issued this critical-severity FDA Drug recall-Presence of Particulate Matter.
Sourced from official FDA Drug enforcement records. Verify recall #D-1697-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-1697-2012) was formally reported on October 3, 2012, with the manufacturer initiating the action on June 26, 2012. It is classified under Critical severity (Class I), with a current status of Terminated. Ben Venue Laboratories Inc is listed as the recalling firm, operating out of Bedford, OH. Federal records list the affected scope as 797 boxes/10/20 mg vials.
The documented reason for this recall is: Presence of Particulate Matter Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Critical
Affected scope
797 boxes/10/20 mg vials
Related Recalls
6
5 from same agency
Vecuronium Bromide for Injection, For IV use only, 20 mg per vial, 10 x 10 mg Vials, lyophilized powder per carton, Rx Only, Mfr. By: Ben Venue Laboratories, Bedford, OH 44146: Mfg for: Bedford Labs, Bedford, OH 44146, NDC 55390-039-10.
Presence of Particulate Matter
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-1697-2012 |
| Date reported | October 3, 2012 |
| Date initiated | June 26, 2012 |
| Recalling firm | Ben Venue Laboratories Inc |
| Firm location | Bedford, OH |
| Affected scope | 797 boxes/10/20 mg vials |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported October 3, 2012. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.