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
Reported: July 13, 2016 Initiated: August 21, 2015 #D-1153-2016
Product Description
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
Details
- Recalling Firm
- Cantrell Drug Company
- Units Affected
- a) 450 syringes and b) 1250 syringes
- Distribution
- Nationwide
- Location
- Little Rock, AR
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Cantrell Drug Company. Units affected: a) 450 syringes and b) 1250 syringes.
Why was this product recalled? ▼
Subpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 13, 2016. Severity: Critical. Recall number: D-1153-2016.
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