Latest Breaking News On - Sedgwick inc - Page 1 : comparemela.com

What s News, Breaking: Thursday, December 28, 2023

What s News, Breaking: Thursday, December 28, 2023
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Hospira, Inc Issues A Voluntary Nationwide Recall For 4 2% Sodium Bicarbonate Injection, 8 4% Sodium Bicarbonate Injection, and Atropine Sulfate Injection Due to the Potential Presence of Glass Particulate Matter

Hospira, Inc., a Pfizer company, is voluntarily recalling the lots listed in the table below of 4.2% Sodium Bicarbonate Injection, USP ABBOJECT® Glass Syringe, 5 mEq/10 mL; 8.4% Sodium Bicarbonate Injection, USP Lifeshield® ABBOJECT® Glass Syringe, 50 mEq/50 mL; and Atropine Sulfate Injection, USP L

United statesPuerto ricoCompany contact informationCompany nameSedgwick incContact centerDrug administrationHospira incCompany announcementAnnouncement dateGlass particulateSodium bicarbonate injectionGlass syringeAtropine sulfate injectionBicarbonate injectionSulfate injection

Hospira, Inc Issues A Voluntary Nationwide Recall For One Lot of Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial Due To The Potential For Presence of Glass Particulate Matter

Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Bleomycin for Injection, USP 15 units Single Dose ONCO-TAIN™ Glass Fliptop Vial, lot BL12206A, to the user level. The recall was initiated due to a confirmed customer report for the presence of glass particulate within a single via

Company contact informationHospira incSedgwick incDrug administrationContact centerCompany announcementCompany nameAnnouncement dateGlass particulateSingle doseGlass fliptopGlass fliptop vialHealthcare professionalsWatch adverse event reportingUnited statesfood

Cardinal Health, Inc Issues Voluntary Nationwide Recall of Certain LEADER™ Brand Eye Drops Supplied by Velocity Pharma, LLC Due to Potential Risk of Eye Infections

Dublin, OH, Cardinal Health, Inc. is initiating a voluntarily recall for all lots of ophthalmic products supplied by Velocity Pharma, LLC to the consumer level. Cardinal Health, Inc. received information from FDA indicating investigators found insanitary conditions in the manufacturing facility and

Erich timmermanDrug administrationCompany nameCompany announcementCardinal health incSedgwick incVelocity pharmaCompany contact informationAnnouncement dateCardinal healthIrritation reliefPolyvinyl alcoholCarboxymethylcellulose sodiumEye reliefPolyethylene glycolPropylene glycol

Hospira, Inc Issues a Voluntary Nationwide Recall for 4 2% Sodium Bicarbonate Injection, USP and 1% and 2% Lidocaine HCl Injection, USP Due to the Potential for Presence of Glass Particulate Matter

Hospira, Inc., a Pfizer company, is voluntarily recalling the lots listed in the table below of 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10mL vial; 1% Lidocaine HCl Injection, USP, 50 mg/5mL vial; and 2% Lidocaine HCl Injection, USP, 100 mg/5mL vial to the user level. The recall was initiated d

Puerto ricoUnited statesCompany announcementCompany contact informationDrug administrationSedgwick incHospira incCompany nameAnnouncement dateSodium bicarbonate injectionBicarbonate injectionHydrochloride injectionLot numberExpiration dateHealthcare professionalsWatch adverse event reporting