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 IIReported ongoing

Distribution: Within the U.S Market.

Official source

Apr 27, 2026FDA 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

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Class IIIReported ongoing

Distribution: USA Nationwide

Official source

Apr 27, 2026FDA 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

Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

Class IIIReported ongoing

Distribution: USA Nationwide

Official source

Nov 26, 2025FDA drug enforcement

Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC 51407-973-10

Presence of Foreign Tablets/Capsules

Class IIReported ongoing

Distribution: Nationwide within the USA

Official source

Oct 20, 2025FDA 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...

Failed Dissolution Specifications

Class IIReported ongoing

Distribution: Nationwide in the USA

Official source

Mar 5, 2025FDA drug enforcement

PRASUGREL TABLETS, 5 mg, 30 tablet bottles, Rx only, packaged by GSMS, Incorporated, Camarillo, CA 93012 NDC 51407-444-30

Failed Dissolution Specifications

Class IIReported ongoing

Distribution: U.S. Nationwide

Official source

May 13, 2024FDA 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,...

CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the proposed interim limit.

Class IIReported terminated

Distribution: Nationwide in the U.S.

Official source

Feb 14, 2024FDA 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 ...

CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex

Class IIReported ongoing

Distribution: Nationwide in the USA

Official source

Jan 12, 2024FDA 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

Failed Dissolution Specifications

Class IIReported terminated

Distribution: Illinois only

Official source

Nov 10, 2023FDA 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...

Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine

Class IIReported terminated

Distribution: Nationwide in the USA

Official source

Nov 10, 2023FDA 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, ...

Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine

Class IIReported terminated

Distribution: Nationwide in the USA

Official source

Nov 10, 2023FDA 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...

Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc. recalling lots due to Out of specification results for the excipient Amadori Glucose adduct of Paroxetine

Class IIReported terminated

Distribution: Nationwide in the USA

Official source

May 25, 2023FDA 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...

Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary container.

Class IIReported terminated

Distribution: Nationwide in the USA

Official source

Oct 6, 2022FDA 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...

Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).

Class IIReported terminated

Distribution: USA nationwide

Official source

Oct 6, 2022FDA 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

Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).

Class IIReported terminated

Distribution: USA nationwide

Official source

Sep 29, 2022FDA 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

Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained Clopidogrel 75mg Tablets

Class IReported terminated

Distribution: USA Nationwide

Official source

Mar 16, 2022FDA 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.

CGMP Deviations

Class IIReported ongoing

Distribution: Nationwide in the U.S: PA, MA, OH, TX, IL, ND, HI

Official source

Mar 16, 2022FDA 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.

CGMP Deviations

Class IIReported ongoing

Distribution: Nationwide in the U.S: PA, MA, OH, TX, IL, ND, HI

Official source

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 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 and the agency's current notices.

Where can I find older records?

Use monthly 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.

Records and reported status

Reasons in these listed records

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