The Compounding Pharmacy of America Recalls Recalls by year
A bar chart of the number of recalls naming this company by year.
Recalls by year
Year Recalls 2015 99 2018 1
Download CSV FDA Recall
Terminated
Historical record Class II
Hydromorphone 60 mg/ml + Fentanyl 20,000 mcg/ml + Bupivacaine 40 mg/ml + Clonidine 1,000 mcg/ml + Baclofen 300 mcg/ml Intrathecal Solution, Sterile-Preservative Free, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Hydromorphone 60 mg/ml + Fentanyl 1,000 mcg/ml + Bupivacaine 10 mg/ml Intrathecal Solution, Sterile-Preservative Free, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Hydromorphone 45 mg/ml + Fentanyl 10,000 mcg/ml + Bupivacaine 15 mg/ml + Baclofen 720 mcg/ml Intrathecal Solution, Sterile-Preservative Free, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Hydromorphone 35 mg/ml + Bupivacaine 4 mg/ml Intrathecal Solution, Sterile-Preservative Free, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Hydromorphone 35 mg/ml + Bupivacaine 10 mg/ml + Baclofen 1,500 mcg/ml + Clonidine 200 mcg/ml Intrathecal Solution, Sterile-Preservative Free, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Hydromorphone 3 mg/ml + Baclofen 2,500 mcg/ml Intrathecal Solution, Sterile-Preservative Free, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Hydromophone 10 mg/ml + Clonidine 300 mcg/ml + Baclofen 120 mcg/ml Intrathecal Solution, Sterile-reservative Free, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Calmme Injectable, Multi-Dose Vial, Sterile, Room Temperature, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Bi-Mix Medium (30/1) Injectable, Sterile, Keep Frozen, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Bi-Mix (20/1) Injectable, Sterile, Keep Frozen, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Bi-Mix #1 (17.365 mg/0.59 mg) Injectable, Sterile, Keep Frozen, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
FDA Recall
Terminated
Historical record Class II
Vancomycin 25 mg/ml Ophthalmic Solution, Single Dose, Sterile, Keep Frozen, The Compounding Pharmacy of America, Knoxville, TN by The Compounding Pharmacy of America
Reason
Lack of Assurance of Sterility; FDA inspection identified GMP violations potentially impacting product quality and sterility Published
September 23, 2015 Distribution
Nationwide
View recall →
This page lists recalls that name The Compounding Pharmacy of America as the recalling firm in the official source notice. It is
not a safety rating, ranking, or statement that the company acted negligently.
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