FDA Drug Recalls

Recalls / Class II

Class IID-0068-2018

Product

ROCuronium Bromide 10 mg per mL, 5 mL Fill in single dose syringe, (50 mg / 5 mL Total Dose) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-850-09

Affected lot / code info
Lot: 20171004@4 BUD: 01/09/2018

Why it was recalled

Lack Of Assurance Of Sterility.

Recalling firm

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

Distribution

Quantity
487 syringes
Distribution pattern
Nationwide in the United States

Timeline

Recall initiated
2017-10-19
FDA classified
2017-11-02
Posted by FDA
2017-11-08
Terminated
2019-05-01
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0068-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls