Total recalls 52 since 2016
Last 12 months 0 reported
Class I 7 13% of total
Ongoing 0 latest 16 Aug 2017
Recalls per month, last 24 months click a bar for that month Severity split
7 13%45 87%0 0%
Why cantrell drug is recalled
All cantrell drug recalls, newest first 52 total Reported Class Recall Company Reason Where 16 Aug 2017 Drug CLASS II Ephedrine Sulfate in 0.9% Sodium Chloride, 50 mg recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Norepinephrine Bitartrate 4 mg Added to 0.9% Sodium recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Diltiazem HCl 125 mg in 5% Dextrose Single-Dose recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Adenosine in 0.9% Sodium Chloride, 90 mg recalled by Cantrell Drug Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Glycopyrrolate Injection Solution 0.4 mg recalled by Cantrell Drug Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Norepinephrine Bitartrate 16 mg Added to 0.9% Sodium recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Succinylcholine Chloride Injection Solution, 100 mg recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Ephedrine Sulfate Injection Solution, 50 mg recalled by Cantrell Drug Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Succinylcholine Chloride Injection Solution, 200 mg recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Sodium Bicarbonate 8.4% Injection Solution, 50 mEq recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Ephedrine Sulfate in 0.9% Sodium Chloride, 25 mg recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Glycopyrrolate Injection Solution 0.2 mg recalled by Cantrell Drug Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Rocuronium Bromide Injection Solution, 50 mg recalled by Cantrell Drug Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Neostigmine Methylsulfate Injection Solution, 5 mg recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Glycopyrrolate Injection Solution 1 mg recalled by Cantrell Drug Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Ephedrine Sulfate in 0.9% Sodium Chloride, 50 mg recalled Cantrell Drug Sterility Nationwide 16 Aug 2017 Drug CLASS II Phenylephrine HCL in 0.9% Sodium Chloride, 1 mg recalled Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Calcium Chloride* Added to 5% Dextrose (20 mg/mL)*, Single-Dose recalled Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Morphine Sulfate 1 mg/mL in 0.9% Sodium Chloride, Single-Dose recalled Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Phenylephrine HCl 1 mg/ (100 mcg/mL) recalled by Cantrell Drug Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride PCA Vial recalled Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Midazolam HCl 50 mg/ in 0.9% Sodium Chloride (1 mg/mL) recalled Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Fentanyl Citrate 2 mcg/mL & Bupivacaine HCl recalled by Cantrell Drug Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Rocuronium Bromide 50 mg/ Injection Solution recalled by Cantrell Drug Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Neostigmine Methylsulfate 5 mg/ Injection Solution recalled Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Glycopyrrolate 1 mg/ (0.2 mg/mL) Injection Solution recalled Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Heparin Sodium 5,000 USP Units Added to 0.9% Sodium recalled Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride recalled Cantrell Drug Sterility Nationwide 21 Dec 2016 Drug CLASS II Succinylcholine Chloride 200 mg/ Injection Solution recalled Cantrell Drug Sterility Nationwide
Load more (22 more)
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.