FDA recall D-1153-2016

Cantrell Drug Company · Class I · drug

Product

Atropine Sulfate Injection Solution, 0.4 mg/1 mL (0.4 mg/mL), in a) 1 mL syringes and b) 2 mL syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-010-45, UPC: 0100352533010453

Reason for recall

Subpotent Drug

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2015-08-21
Report date
2016-07-13
Termination date
2017-02-03
Voluntary/Mandated
Voluntary: Firm initiated
Location
Little Rock, AR, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1153-2016