FDAFDA · Food and drugs·Recall number D-1017-2017
Hydromorphone 0.5 mg/mL in 0.9% Sodium Chloride 1 mL Fill in 3 mL BD syringe, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0302-05
Published August 2, 2017 · Recall initiated: July 14, 2017
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
Lack of Assurance of Sterility; product has the potential to leak.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- SCA Pharmaceuticals
- Distributor
- Nationwide
- Lot
- Lot: 20170508@75 BUD: 8/6/2017
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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