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Golden State Medical Supply Inc.

Recalls

Recalls by year

A bar chart of the number of recalls naming this company by year.

Recalls by year
YearRecalls
20141
20153
20167
20183
201911
20204
20213
20228
20234
20243
20253
20263
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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets USP 25 mg 1000 count bottle NDC 60429-316-10 Rx only GSMS Incorporated

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer
Published
May 29, 2019
Distribution
IL, MI, MN, PA, TN, TX. Two (2) US gover…

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets USP 25 mg 90 count bottle NDC 60429-316-90 Rx only GSMS Incorporated

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer
Published
May 29, 2019
Distribution
IL, MI, MN, PA, TN, TX. Two (2) US gover…

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets USP 25 mg 30 count bottle NDC 60429-316-30 Rx only GSMS Incorporated

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer
Published
May 29, 2019
Distribution
IL, MI, MN, PA, TN, TX. Two (2) US gover…

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FDA Recall Terminated Historical recordClass II

IRBESARTAN Tablets, USP 300 mg (a) 30-count bottle (NDC 60429-642-30), (b) 90-count bottle (NDC 60429-642-90) Rx Only, Manufactured by: SciGen Pharmaceuticals, Inc. Hauppauge, NY 11788, Distributed by: GSMS, Incorporated, Camarillo, CA 93012, USA.

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodiethylamine (NDEA) in product.
Published
November 28, 2018
Distribution
Product was distributed throughout the U…

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FDA Recall Terminated Historical recordClass II

IRBESARTAN Tablets, USP 150 mg (a) 30-count bottle (NDC 60429-641-30), (b) 90-count bottle (NDC 60429-641-90) Rx Only, Manufactured by: SciGen Pharmaceuticals, Inc. Hauppauge, NY 11788, Distributed by: GSMS, Incorporated, Camarillo, CA 93012, USA.

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodiethylamine (NDEA) in product.
Published
November 28, 2018
Distribution
Product was distributed throughout the U…

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FDA Recall Terminated Historical recordClass II

IRBESARTAN Tablets, USP 75 mg 90-count bottle, Rx Only, Manufactured by: SciGen Pharmaceuticals, Inc. Hauppauge, NY 11788, Distributed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC 60429-640-90.

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodiethylamine (NDEA) in product.
Published
November 28, 2018
Distribution
Product was distributed throughout the U…

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FDA Recall Terminated Historical recordClass II

Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx Only, GSMS, NDC # 60429-122-90

by Golden State Medical Supply Inc.

Reason
Failed Dissolution Specifications: Out-of-specification results in retained sample.
Published
August 24, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) 30 capsules per bottle, NDC # 60429-123-30, b) 90 capsules per bottle, NDC # 60429-123-90, Rx Only, GSMS.

by Golden State Medical Supply Inc.

Reason
Failed Dissolution Specifications: Out-of-specification results in retained sample.
Published
August 24, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

DULOXETINE Delayed-Release Capsules, USP, 60 mg, 1000 count bottles, Rx only, Manufactured by: Laboratorios del Dr. Esteve, SA, Martorelles, Barcelona --- NDC 60429-166-10

by Golden State Medical Supply Inc.

Reason
Labeling; Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on container label is 02/2019, correct expiration date should be 02/2018
Published
July 20, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium 80 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-326-77

by Golden State Medical Supply Inc.

Reason
Failed Impurities/Degradation Specifications
Published
March 16, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium 40 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-325-77

by Golden State Medical Supply Inc.

Reason
Failed Impurities/Degradation Specifications
Published
March 16, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium 20 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-324-77

by Golden State Medical Supply Inc.

Reason
Failed Impurities/Degradation Specifications
Published
March 16, 2016
Distribution
Nationwide

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This page lists recalls that name Golden State Medical Supply Inc. as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.