FDAFDA · Food and drugs·Recall number D-925-2013
Benztropine Mesylate Injection, USP, 2 mg/mL(1 mg/1 mL), 2 mL Single Dose Vial, Rx only, Manufactured in the USA for Nexus Pharmaceuticals Inc, Lincolnshire, IL 60069, NDC 14789-300-02
Published September 4, 2013 · Recall initiated: August 1, 2013
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
Presence of particulate matter: characterized as thin colorless flakes that are visually and chemically consistent with glass delamination.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Nexus Pharmaceuticals Inc
- Distributor
- Nationwide
- Lot
- a) Lot: 112911, Exp. 11/13, b) Lot: 030712, Exp. 3/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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