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Golden State Medical Supply Inc.

Golden State Medical Supply Inc. Recalls

All product recalls associated with Golden State Medical Supply Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 21–40 of 21319 recalls

Baclofen Tablets (Golden State) – Foreign Tablet Presence (2025)

Presence of Foreign Tablets/Capsules

Class IIModerate

FDANov 26, 2025Nationwide• Golden State Medical Supply Inc.

Cisatracurium Besylate Injection (Somerset) – Subpotent Product (2025)

Subpotent product:out of specification assay results observed during long term stability testing.

Class IIILow

FDANov 26, 2025Nationwide• SOMERSET THERAPEUTICS LLC

LifeShield Drug Library Management (DLM), LifeShield Infu... (ICU Medical, Inc.) – software issue only allows concentrat... (2025)

Software issue only allows Concentration Limits to be defined to one digit of precision past the decimal point (0.1) instead of three digits (0.001). If the user is unable to use Concentration Limits as intended, they may need to change the limits to something other than what is recommended by the drug manufacturer, which may result in over- or under-delivery.

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High

FDANov 24, 2025Nationwide• ICU Medical, Inc.

Zimmer Air Dermatome, Model/Catalog Number: 00880100100 (Zimmer Surgical Inc) – the devices may have a misaligned thi... (2025)

The devices may have a misaligned thickness control bar.

Moderate

FDANov 24, 2025Nationwide• Zimmer Surgical Inc

LifeShield Drug Library Management (DLM); LifeShield Infu... (ICU Medical, Inc.) – for certain customers, the change sum... (2025)

For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed. Users must use alternate methods to review changes. Failure to do so may lead in over delivery, under delivery, or delay in setup on the infusion pump.

High

FDANov 24, 2025Nationwide• ICU Medical, Inc.

Duloxetine Capsules (Breckenridge) – Impurity Limit Exceeded (2025)

CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit

Class IIModerate

FDANov 24, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

Zimmer Dermatome AN, Model/Catalog Number: 88710100 (Zimmer Surgical Inc) – the devices may have a misaligned thi... (2025)

The devices may have a misaligned thickness control bar.

Moderate

FDANov 24, 2025Nationwide• Zimmer Surgical Inc

Duloxetine Capsules (Breckenridge) – Impurity Limit Exceeded (2025)

CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit

Class IIModerate

FDANov 24, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

The Elecsys Anti-TSHR immunoassay is a three-step competi... (Roche Diagnostics Operations, Inc.) – issues identified: 1) results vary by... (2025)

Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as delay of treatment or incorrect treatment.

High

FDANov 21, 2025Nationwide• Roche Diagnostics Operations, Inc.

Bisoprolol/Hydrochlorothiazide Tablets (Glenmark) – Cross Contamination (2025)

Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe

Class IIILow

FDANov 21, 2025Nationwide• Glenmark Pharmaceuticals Inc., USA

Magnet Fidget Spinner Sets (Anzmtosn) – magnet ingestion (2025)

This recall involves Anzmtosn Magnet Fidget Spinner Sets. Each set contains 15 pieces and comes with four iridescent oval-shaped magnets, eight iridescent cuboidal-shaped magnetic stones, one red and yellow disk-shaped metal fidget spinner, one winged metal fidget spinner, and one multicolored infinity fidget cube. The set comes with a black fabric-lined storage case. The batch number, CCA06582, is printed on the back label of the packaging.

Very High

CPSCNov 20, 2025Nationwide• Shenzhenshibangduoladianzikejimaoyi Co., Ltd. (Shenzhen Bangduola Electronic Technology Trade Co., Ltd.), of China

Restore Clinician Programmer Application (CP App), Model ... (Medtronic Neuromodulation) – software issue where a device reset m... (2025)

Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and the patient experienced a recurrence of underlying pain symptoms. Resolution would require surgical replacement of the INS.

Moderate

FDANov 20, 2025Nationwide• Medtronic Neuromodulation

Tropicamide Ophthalmic Solution (Fagron) – Incorrect Formulation (2025)

Incorrect Product Formulation

Class IIModerate

FDANov 20, 2025Nationwide• Fagron Compounding Services

Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Ca... (Vortex Surgical Inc.) – reason for the voluntary recall is so... (2025)

Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.

Moderate

FDANov 19, 2025Nationwide• Vortex Surgical Inc.

Hardware configuration of the BeneVision Central Monitori... (Mindray DS USA, Inc. dba Mindray North America) – when the worstation of the benevision... (2025)

When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.

Moderate

FDANov 18, 2025Nationwide• Mindray DS USA, Inc. dba Mindray North America

Intelerad InteleShare software, with ProViewer component (DICOM Grid, Inc.) – software intended to aid in diagnosin... (2025)

Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing images in InteleShare viewer; Multiplanar reconstruction applied; Manual rotation applied, could result in inaccurate length measurement tool values that could compromise diagnostic accuracy, lead to misdiagnosis or inappropriate follow-up.

High

FDANov 18, 2025AL, AK, AZ +42 more• DICOM Grid, Inc.

Nebivolol Tablets (Glenmark) – Cross Contamination (2025)

Cross Contamination with Other Products

Class IIILow

FDANov 18, 2025Nationwide• Glenmark Pharmaceuticals Inc., USA

Ondansetron ODT Tablets (Preferred) – Defective Packaging (2025)

Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale.

Class IIModerate

FDANov 17, 2025IN• Preferred Pharmaceuticals, Inc.

Orthofix NorthStar OCT Navigation Surgical Technique Guid... (SEASPINE ORTHOPEDICS CORPORATION) – the northstar oct navigation surgical... (2025)

The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as compatible with the NorthStar OCT Navigation Instruments. However, the NorthStar OCT Navigation Instruments are compatible for use with Medtronic s Solera toolcards only.

Moderate

FDANov 17, 2025AL, AZ, CA +21 more• SEASPINE ORTHOPEDICS CORPORATION

Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST01... (AVID Medical, Inc.) – potential for incomplete seal on head... (2025)

Potential for incomplete seal on header bag.

Moderate

FDANov 14, 2025GA, IL, MD +1 more• AVID Medical, Inc.