--- title: "Golden State Medical Supply Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Golden State Medical Supply Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/golden-state-medical-supply-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Golden State Medical Supply Inc. recall records **13** reported ongoing 25 records in this archive. Latest source date Aug 21, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 21, 2026 FDA drug enforcement ### [Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC: 51407-445-30.](https://isitonrecall.com/recall/fda-drug-d-0847-2026-prasugrel-hci-tablets-usp-10mg-30-count-bottle-rx-only-marketed-by-gsms-incorporated-camarillo-ca-93/) Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution Class II Reported ongoing Distribution: US Nationwide. [Official source for Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Cam...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0847-2026%22) Aug 7, 2026 FDA drug enforcement ### [Carbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-215-10), b) 100-count bottles (NDC 51407-215-01), Rx Only, Manufactured by: Taro Pharmaceutical In...](https://isitonrecall.com/recall/fda-drug-d-0771-2026-carbamazepine-tablets-usp-200mg-packaged-in-a-1000-count-bottles-ndc-51407-215-10-b-100-count-bottle/) CGMP deviations: tablets with black specks. Class II Reported ongoing Distribution: USA Nationwide [Official source for Carbamazepine Tablets, USP, 200mg, packaged in a)1000-count bottles (NDC 51407-215-10), b) 100-co...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0771-2026%22) May 29, 2026 FDA drug enforcement ### [GSMS Incorporated, NIACIN EXTENDED-RELEASE TABLETS, USP, 1,000 MG, 90 tablets, Rx only, Manufactured by Kremers Urban Pharmaceuticals Inc., a subsidiary of Lannett, Inc., Seymou...](https://isitonrecall.com/recall/fda-drug-d-0587-2026-gsms-incorporated-niacin-extended-release-tablets-usp-1-000-mg-90-tablets-rx-only-manufactured-by-kr/) Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour timepoint. Class II Reported ongoing Distribution: Within the U.S Market. [Official source for GSMS Incorporated, NIACIN EXTENDED-RELEASE TABLETS, USP, 1,000 MG, 90 tablets, Rx only, Manufactu...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0587-2026%22) Apr 27, 2026 FDA drug enforcement ### [Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-637-05](https://isitonrecall.com/recall/fda-drug-d-0534-2026-primidone-tablets-usp-50-mg-50-count-bottle-rx-only-manufactured-by-lannett-company-inc-marketed-by/) Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. Class III Reported ongoing Distribution: USA Nationwide [Official source for Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0534-2026%22) Apr 27, 2026 FDA drug enforcement ### [Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01](https://isitonrecall.com/recall/fda-drug-d-0535-2026-primidone-tablets-usp-250-mg-100-count-bottle-rx-only-manufactured-by-lannett-company-inc-marketed-b/) Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. Class III Reported ongoing Distribution: USA Nationwide [Official source for Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc....](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0535-2026%22) Nov 26, 2025 FDA drug enforcement ### [Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC 51407-973-10](https://isitonrecall.com/recall/fda-drug-d-0235-2026-baclofen-tablets-usp-10-mg-1000-count-bottles-rx-only-marketed-by-gsms-incorporated-ca-93012-usa-ndc/) Presence of Foreign Tablets/Capsules Class II Reported ongoing Distribution: Nationwide within the USA [Official source for Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 930...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0235-2026%22) Oct 20, 2025 FDA drug enforcement ### [NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: Kremers Urban Pharmaceuticals, Inc., a subsidiary of Lannett Company, Inc., Seym...](https://isitonrecall.com/recall/fda-drug-d-0158-2026-niacin-extended-release-tablets-usp-1-000-mg-90-tablets-per-bottle-rx-only-manufactured-by-kremers-u/) Failed Dissolution Specifications Class II Reported ongoing Distribution: Nationwide in the USA [Official source for NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0158-2026%22) Mar 5, 2025 FDA drug enforcement ### [PRASUGREL TABLETS, 5 mg, 30 tablet bottles, Rx only, packaged by GSMS, Incorporated, Camarillo, CA 93012 NDC 51407-444-30](https://isitonrecall.com/recall/fda-drug-d-0287-2025-prasugrel-tablets-5-mg-30-tablet-bottles-rx-only-packaged-by-gsms-incorporated-camarillo-ca-93012-nd/) Failed Dissolution Specifications Class II Reported ongoing Distribution: U.S. Nationwide [Official source for PRASUGREL TABLETS, 5 mg, 30 tablet bottles, Rx only, packaged by GSMS, Incorporated, Camarillo, C...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0287-2025%22) May 13, 2024 FDA drug enforcement ### [Duloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, a) 30 capsules bottles, NDC 60429-165-30; b) 90 capsules bottles, NDC 60429-165-90, Mfr. by: Towa Pharmaceutical Europe,...](https://isitonrecall.com/recall/fda-drug-d-0568-2024-duloxetine-delayed-release-capsules-usp-30mg-rx-only-a-30-capsules-bottles-ndc-60429-165-30-b-90-cap/) CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the proposed interim limit. Class II Reported terminated Distribution: Nationwide in the U.S. [Official source for Duloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, a) 30 capsules bottles, NDC 60429-165-30...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0568-2024%22) Feb 14, 2024 FDA drug enforcement ### [Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 g net fill, Rx only, Manufactured by: Apotek Inc., Toronto, Ontario, Cananda, Marketed by: GSMS ...](https://isitonrecall.com/recall/fda-drug-d-0349-2024-fluticasone-propionate-nasal-spray-usp-50-mcg-per-spray-120-metered-sprays-16-g-net-fill-rx-only-man/) CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex Class II Reported ongoing Distribution: Nationwide in the USA [Official source for Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 g net fill, Rx o...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0349-2024%22) Jan 12, 2024 FDA drug enforcement ### [Budesonide Extended-Release Tablets, 9 mg, 30-count bottles, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA, UPC 5140782430, NDC 51407-824-30](https://isitonrecall.com/recall/fda-drug-d-0276-2024-budesonide-extended-release-tablets-9-mg-30-count-bottles-rx-only-marketed-by-gsms-incorporated-cama/) Failed Dissolution Specifications Class II Reported terminated Distribution: Illinois only [Official source for Budesonide Extended-Release Tablets, 9 mg, 30-count bottles, Rx only, Marketed by: GSMS, Incorpor...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0276-2024%22) Nov 10, 2023 FDA drug enforcement ### [PAROXETINE tablets, USP, 10 mg, Packaged as a) 30-count bottle, NDC 60429-734-30; b) 90-count bottle NDC 60429-734-90; c)1000-count bottle, NDC 60429-734-10; Rx Only, Manufactur...](https://isitonrecall.com/recall/fda-drug-d-0128-2024-paroxetine-tablets-usp-10-mg-packaged-as-a-30-count-bottle-ndc-60429-734-30-b-90-count-bottle-ndc-60/) Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine Class II Reported terminated Distribution: Nationwide in the USA [Official source for PAROXETINE tablets, USP, 10 mg, Packaged as a) 30-count bottle, NDC 60429-734-30; b) 90-count bot...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0128-2024%22) Nov 10, 2023 FDA drug enforcement ### [PAROXETINE tablets, USP, 20 mg, Packaged as a) 90-count bottle NDC 60429-735-90; b)1000-count bottle, NDC 60429-735-10; Rx Only, Manufactured by Apotex, Inc., Toronto, Ontario, ...](https://isitonrecall.com/recall/fda-drug-d-0129-2024-paroxetine-tablets-usp-20-mg-packaged-as-a-90-count-bottle-ndc-60429-735-90-b-1000-count-bottle-ndc/) Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine Class II Reported terminated Distribution: Nationwide in the USA [Official source for PAROXETINE tablets, USP, 20 mg, Packaged as a) 90-count bottle NDC 60429-735-90; b)1000-count bot...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0129-2024%22) Nov 10, 2023 FDA drug enforcement ### [PAROXETINE tablets, USP, 40 mg, Packaged as a) 30-count bottle, NDC 60429-737-30; b) 90-count bottle NDC 60429-737-90; c)1000-count bottle, NDC 60429-737-10; Rx Only, Manufactur...](https://isitonrecall.com/recall/fda-drug-d-0130-2024-paroxetine-tablets-usp-40-mg-packaged-as-a-30-count-bottle-ndc-60429-737-30-b-90-count-bottle-ndc-60/) Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine Class II Reported terminated Distribution: Nationwide in the USA [Official source for PAROXETINE tablets, USP, 40 mg, Packaged as a) 30-count bottle, NDC 60429-737-30; b) 90-count bot...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0130-2024%22) May 25, 2023 FDA drug enforcement ### [Travoprost Ophthalmic Solution, USP (Ionic Buffered Solution), 0.004%, Rx only, Manufactured by Apotex Inc., Manufactured by: GSMS Incorporated, Camarillo, CA 93012, a) NDC 5140...](https://isitonrecall.com/recall/fda-drug-d-0867-2023-travoprost-ophthalmic-solution-usp-ionic-buffered-solution-0-004-rx-only-manufactured-by-apotex-inc/) Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary container. Class II Reported terminated Distribution: Nationwide in the USA [Official source for Travoprost Ophthalmic Solution, USP (Ionic Buffered Solution), 0.004%, Rx only, Manufactured by A...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0867-2023%22) Oct 6, 2022 FDA drug enforcement ### [Rifampin Capsules, USP, 300 mg, packaged in a) 30-count bottle (NDC 51407-323-30), b) 60-count bottle (NDC 51407-323-60), c) 100-count bottle (NDC 51407-323-01), Rx only, Manufa...](https://isitonrecall.com/recall/fda-drug-d-0011-2023-rifampin-capsules-usp-300-mg-packaged-in-a-30-count-bottle-ndc-51407-323-30-b-60-count-bottle-ndc-51/) Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP). Class II Reported terminated Distribution: USA nationwide [Official source for Rifampin Capsules, USP, 300 mg, packaged in a) 30-count bottle (NDC 51407-323-30), b) 60-count bo...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0011-2023%22) Oct 6, 2022 FDA drug enforcement ### [Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA, NDC 51407-322-30](https://isitonrecall.com/recall/fda-drug-d-0012-2023-rifampin-capsules-usp-150-mg-30-count-bottle-rx-only-manufactured-by-patheon-pharmaceuticals-inc-oh/) Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP). Class II Reported terminated Distribution: USA nationwide [Official source for Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0012-2023%22) Sep 29, 2022 FDA drug enforcement ### [Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY LTD, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC 60429-027-10](https://isitonrecall.com/recall/fda-drug-d-0019-2023-atenolol-tablets-usp-25-mg-1000-count-bottle-rx-only-manufactured-by-alphapharm-pty-ltd-marketed-by/) Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets Class I Reported terminated Distribution: USA Nationwide [Official source for Atenolol Tablets, USP, 25 mg, 1000-count bottle, Rx only, Manufactured by: ALPHAPHARM PTY LTD, Ma...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0019-2023%22) Mar 16, 2022 FDA drug enforcement ### [Enalapril Maleate Tablets, USP; 2.5 mg; 90 tablets, NDC 60429-183-90; manufactured by Taro Pharmaceutical Industries, Ltd.; packaged by GSMS, Incorporated, CA, USA.](https://isitonrecall.com/recall/fda-drug-d-1177-2022-enalapril-maleate-tablets-usp-2-5-mg-90-tablets-ndc-60429-183-90-manufactured-by-taro-pharmaceutical/) CGMP Deviations Class II Reported ongoing Distribution: Nationwide in the U.S: PA, MA, OH, TX, IL, ND, HI [Official source for Enalapril Maleate Tablets, USP; 2.5 mg; 90 tablets, NDC 60429-183-90; manufactured by Taro Pharma...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1177-2022%22) Mar 16, 2022 FDA drug enforcement ### [Enalapril Maleate Tablets, USP; 5 mg; 90 tablets, NDC 60429-184-90; manufactured by Taro Pharmaceutical Industries, Ltd.; packaged by GSMS, Incorporated, CA.](https://isitonrecall.com/recall/fda-drug-d-1178-2022-enalapril-maleate-tablets-usp-5-mg-90-tablets-ndc-60429-184-90-manufactured-by-taro-pharmaceutical-i/) CGMP Deviations Class II Reported ongoing Distribution: Nationwide in the U.S: PA, MA, OH, TX, IL, ND, HI [Official source for Enalapril Maleate Tablets, USP; 5 mg; 90 tablets, NDC 60429-184-90; manufactured by Taro Pharmace...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1178-2022%22) ## Reasons in these listed records - Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution - CGMP deviations: tablets with black specks. - Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour timepoint. - Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. These examples come from this result page and are not a ranking of every recall reason. ## Checking Golden State Medical Supply Inc. ### Is there a recall on golden state medical supply inc. right now? This archive contains 25 records, including 13 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Golden State Medical Supply Inc.](https://isitonrecall.com/check/?q=Golden%20State%20Medical%20Supply%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)