FDA Drug Recalls

Recalls / Class II

Class IID-0204-2017

Product

Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL) ,Single-Dose Syringe Injection Solution, For Slow IV Use Only ,Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-067-12

Affected lot / code info
Lot: 169262 BUD: 1/8/2017, Lot: 169812 BUD: 1/19/2017

Why it was recalled

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Recalling firm

Firm
Cantrell Drug Company
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
7321 Cantrell Rd, Little Rock, Arkansas 72207-4144

Distribution

Quantity
9859 syringes
Distribution pattern
Nationwide

Timeline

Recall initiated
2016-11-18
FDA classified
2016-12-13
Posted by FDA
2016-12-21
Terminated
2020-04-29
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0204-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.