GILEAD SCIENCES, INC. — Federal Records

co_sos 1 records

CO Business: GILEAD SCIENCES, INC. 2001-05-24

FPC | Status: Good Standing | Foster City, CA

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courtlistener_docket 4 records

Ju v. GILEAD SCIENCES, INC. 2026-06-03

Federal docket 2:26-cv-06480 (njd); matched party 'GILEAD SCIENCES, INC.'

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Levitan v. Gilead Sciences Inc. 2026-04-17

Federal docket 1:26-cv-02329 (nyed); matched party 'Gilead Sciences Inc.'

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Gilead Sciences, Inc. v. Pain Relief Rx, Inc. 2026-04-14

Federal docket 1:26-cv-02172 (nyed); matched party 'Gilead Sciences, Inc.'

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GILEAD SCIENCES, INC. v. SABA ILAC SANAYI VE TICARET A.S. 2026-03-27

Federal docket 2:26-cv-03282 (njd); matched party 'GILEAD SCIENCES, INC.'

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fda 7 records

FDA Drug Recall: Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manu 2024-10-09

Class I — Presence of Particulate Matter: Presence of glass particle.

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FDA Drug Recall: Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manu 2022-01-05

Class I — Presence of Particulate Matter: investigation into a customer complaint confirmed the presence of glass particulates.

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FDA Drug Recall: Emtriva (emtricitabine) Oral Solution, 10 mg/mL, 170 mL bottles, Rx only, Manufa 2014-11-05

Class II — Defective Container; leaking around the cap

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FDA Drug Recall: Truvada (200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate) tablets, 2014-10-15

Class III — Presence of Foreign Substance: Truvada was found to contain small red silicone rubber particulates.

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FDA Drug Recall: Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil fumarate 3 2014-03-05

Class III — Presence of Foreign Substance: Red Silicone Rubber Particulates are Present in Drug.

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FDA Drug Recall: AmBisome (amphotericin B) liposome for Injection, 50 mg, For Intravenous Infusio 2013-07-31

Class II — Lack of Sterility Assurance; During a routine simulation of the manufacturing of AmBisome, a bacterial contamination was detected in some media fill units. No contaminated batches have actu...

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FDA Drug Recall: Vistide (cidofovir) Injection, 375 mg (75 mg/mL), 5 mL single-use vial, Rx only, 2013-05-22

Class I — Presence of Particulate Matter: Particulate matter was found in some vials of Vistide (cidofovir injection).

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fda_adverse 2 records

FDA AE Manufacturer: Gilead Sciences, Inc.

Drug adverse event reporter — Product: LETAIRIS

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FDA AE Manufacturer: Gilead Sciences, Inc

Drug adverse event reporter — Product: TRUVADA

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lobbying 13 records

Lobbying Firm: GILEAD SCIENCES, INC.

Registered lobbying firm — FOSTER CITY, CA

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