FDAFDA · Food and drugs·Recall number D-1550-2020
Heparin Sodium 2,500 units in 0.9% Sodium Chloride 500 mL, Single Dose Container, Rx Only Injection for Intravenous Use (5 units/mL), SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC#: 70004-0655-44, Bar Code 70004065544.
Published September 2, 2020 · Recall initiated: July 29, 2020
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
Cross Contamination with Other Product(s): containers labeled as having methylparaben and propylparaben as preservatives, actually contained undeclared benzyl alcohol and did not contain any parabens.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- SCA Pharmaceuticals
- Distributor
- Nationwide within the U.S.
- Lot
- Lot #: 1220019269, 1220019278, Exp 08/21/2020; 1220019386, Exp 08/25/2020.
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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