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27072 Southwest Ballston Road, Sheridan, Oregon, United States
Updated: February 10, 2022 12:00 PM
245 employees tested positive for Covid-19 at Sheridan Federal Correctional Institution in Yamhill County. Investigation Start Date: 24-01-2022, with the most recent onset of: 29-01-2022 New Cases of: 245
Source: www.oregon.gov See Less
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161 employees tested positive for Covid-19 at Sheridan Federal Correctional Institution in Yamhill County. Investigation Start Date: 7/29/2021, with the most recent onset of: 9/25/2021 New Cases of: 161
Source: www.oregon.gov See Less
3
84 employees tested positive for Covid-19 at Sheridan Correctional Institution in Yamhill County. Investigation Start Date: 2020-10-19with the most recent onset of: 2021-03-31 New Cases of: 84
Source: www.oregon.gov See Less
3
Covid-19 OSHA Complaint, Federal Bureau of Prisons, 27072 BALLSTON ROAD, SHERIDAN, OR, 97378, USA
3 years ago
At the guard temperature check area, employees are loosely wearing scarfs that repeatedly fall down. The guards get belligerent with individuals who question the effectiveness of the loose scarfs.
Alleged Hazards: 1, Employees Exposed: 500
Source: Osha.gov | Receipt Date: 2020-12-08 See Less
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Par Pharmaceutical Treprostinil Injection - recalled due to Silicone Particulate Matter, USA
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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 particulates in the product... See More solution. The lot was distributed nationwide to wholesalers and hospitals from June 16, 2022, through October 17, 2022. To date, Par has not received any reports of adverse events related to this recall.
Administration of an injectable product that contains particulate matter may result in local irritation or swelling in response to the foreign material. If the particulate matter reaches the blood vessels it can travel to various organs and block blood vessels in the heart, lungs, or brain which can cause stroke and even lead to death.
Treprostinil Injection is formulated for subcutaneous or intravenous infusion. The product is a prostacyclin vasodilator indicated for the treatment of pulmonary arterial hypertension to diminish symptoms associated with exercise and for patients who require a transition from epoprostenol to reduce the rate of clinical deterioration.
Treprostinil Injection 20mg/20mL (1mg/mL) is distributed in 20mL multidose vials as sterile solutions in water for injection, individually packaged in cartons under NDC #42023-206-01. Only Lot 57014, expiration date 04/2024 is affected by this recall. Vials from the affected lot bear the attached label.
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In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Endo International, Par Pharmaceutical
Brand name: Par Pharmaceutical
Product recalled: Treprostinil 20mg/20mL Injection
Reason for the recall: Potential Presence of Silicone Particulate Matter
FDA Recall date: March 12, 2024
Source: fda.gov See Less
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