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Covid-19 OSHA Complaint
2 years ago
1. Employees are at risk of exposure to COVID-19 due to failing to self-isolate after working in proximity to employees waiting for COVID-19 test results or employees who were in close contact with someone who tested positive. 2. Employees are at risk of exposure to COVID-19 due... See More to lack of sanitizing after employees were in close contact to someone who tested positive for COVID-19. 3. Employees are at risk of exposure to COVID-19 due to employees returning from vacations outside the Commonwealth of Massachusetts are not self-isolating as recommended by the CDC and Commonwealth of Massachusetts. 4. Employees are at risk of exposure to COVID-19 due to lack of PPE (gloves) while working in the window.
Alleged Hazards: 4, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-04-27 See Less
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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.
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Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
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
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