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Par Pharmaceutical Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution

Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulate

Linda hussCompany nameWinmar incCompany contact informationDrug administrationEndo internationalCompany announcementAnnouncement dateSilicone particulatePar pharmaceuticalTreprostinil injectionWatch adverse event reporting

Par Pharmaceutical (ENDPQ) Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection

Par Pharmaceutical (ENDPQ) Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection
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Drug administrationWinmar incEndo internationalPar pharmaceuticalTreprostinil injectionWatch adverse event reporting

Par Pharmaceutical Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution

DUBLIN, March 12, 2024 /PRNewswire/ Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. , is voluntarily recalling one lot of Treprostinil.

Winmar incDrug administrationPrnewswire endo internationalEndo internationalExchange commissionPar pharmaceuticalTreprostinil injectionOnly lotWatch adverse event reportingPrivate securities litigation reform actAnnual report

Par Pharmaceutical Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution

Par Pharmaceutical Issues Voluntary Nationwide Recall of One Lot of Treprostinil Injection Due to Potential for Silicone Particulates in the Product Solution
streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.

Exchange commissionEndo internationalPrnewswire endo internationalWinmar incDrug administrationPar pharmaceuticalTreprostinil injectionOnly lotWatch adverse event reportingPrivate securities litigation reform actAnnual report

Megadyne Reiterates Intended Use Population Change for Megadyne Mega Soft Universal and Universal Plus Patient Return Electrodes

Megadyne issued a Class 1 Medical Device Correction to hospitals to limit the use of MEGA SOFT Universal and Universal Plus Reusable Patient Return Electrodes to patients aged 12 years or older after receiving reports of adult and pediatric patient burns following surgical procedures in which MEGA S

United statesCompany contact informationMegadyne medical products incEthicon resource departmentCompany announcementCompany nameAnnouncement dateMedical productsSoft universalUniversal plus reusable patient returnDevice correctionUniversal plus reusable patient return electrodesUniversal plusUniversal patient returnUniversal dual patient returnUniversal plus patient return