FDA Drug Recalls

Recalls / Class II

Class IID-0876-2017

Product

ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 2g, Total Approximate Volume 100 mL, Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0522-32

Affected lot / code info
LOT # 20170510@12, Use By: 06-24-17

Why it was recalled

Lack of assurance of sterility: Product bags leaking at seam.

Recalling firm

Firm
SCA Pharmaceuticals
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
8821 Knoedl Ct, Little Rock, Arkansas 72205-4600

Distribution

Quantity
240 bags
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2017-05-18
FDA classified
2017-05-31
Posted by FDA
2017-06-07
Terminated
2018-03-29
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0876-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.