fentaNYL citrate in 0.9% Sodium Chloride Injection, 5 mcg/1 mL (5 mcg/mL), in a) 1 mL syringe (NDC 52533-214-45, UPC: 0100352533214455) and b) 3 mL syringe (NDC 52533-214-60, UPC: 0100352533214608), Rx Only, Cantrell Drug Co., Little Rock, AR
Reported: July 13, 2016 Initiated: August 21, 2015 #D-1156-2016
Product Description
fentaNYL citrate in 0.9% Sodium Chloride Injection, 5 mcg/1 mL (5 mcg/mL), in a) 1 mL syringe (NDC 52533-214-45, UPC: 0100352533214455) and b) 3 mL syringe (NDC 52533-214-60, UPC: 0100352533214608), Rx Only, Cantrell Drug Co., Little Rock, AR
Reason for Recall
Subpotent Drug
Details
- Recalling Firm
- Cantrell Drug Company
- Units Affected
- a) 564 syringes and b) 1146 syringes
- Distribution
- Nationwide
- Location
- Little Rock, AR
Frequently Asked Questions
What product was recalled? ▼
fentaNYL citrate in 0.9% Sodium Chloride Injection, 5 mcg/1 mL (5 mcg/mL), in a) 1 mL syringe (NDC 52533-214-45, UPC: 0100352533214455) and b) 3 mL syringe (NDC 52533-214-60, UPC: 0100352533214608), Rx Only, Cantrell Drug Co., Little Rock, AR. Recalled by Cantrell Drug Company. Units affected: a) 564 syringes and b) 1146 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-1156-2016.
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