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HomeLIFESTAR PHARMA LLC › Sodium Chloride Inhalation Solution, USP, 7%-4mL

Sodium Chloride Inhalation Solution, USP, 7%-4mL

LIFESTAR PHARMA LLC · Model 4mL · UDI-DI 00370756664604

CAF Prescription
1
510(k) clearances
3,131
Adverse events (43 deaths)
36
Recalls
190
Facilities

Description

Carton with 60 vials; 7% Sodium chloride inhalation solution, made to USP, 4mL vial, sterile, preservative free, non-pyrogenic.

Recalls

DateFirmReason
2023-08-04MEDLINE INDUSTRIES, LP - NorthfieldProduct dispositioned for scrap for sterility failure investigation that was inadvertently shipped to customers.
2021-03-31Smiths Medical ASD Inc.The firm became aware via complaints that one lot of ACE MDI Spacers with Small Masks and one lot of Palm Cups (Large) may have incorrect shipping box labels.
2018-08-29SANRAI INTERNATIONAL LLCThe product was designed for 120V usage and is being used in South Africa with 220V. There is a potential for the device to overheat and the mouthpiece can pop off.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.
2017-09-05Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical CompanyLack of sterility assurance: leaking containers which could lead to exposure to infectious agents.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.