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