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Doordash

Updated: December 29, 2021 12:00 PM
Potential concerns with employees required to work who are Covid 19 positive. Reverence Title 8 CCR Section 3203 and 3205

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-10-20 See Less
112


Last night I got woke up at 1 am by a banging on my door. I go to answer it and a car is pulling away from my house. I look down to see a Wendy’s bag and a soda. It’s raining outside . I am like... See More what the hell! I never order food.. thinking it’s a joke I bring it in my house and sit on the counter as of course I am not eating this food. I go back to sleep . 45 minutes later, now 2am someone is banging on my door again. My dogs are going crazy..now I am sooo pissed I am yelling not nice stuff. I tell my hubby you get it. After 5 minutes he gets up and gets dressed. I could still hear the banging. As soon as he opens the door the car pulls away. I am assuming it’s the delivery driver wanting their wet bag of food.
This is not ok!!!!!!!!! You really think it’s ok to bang on someone’s door at 2 am? Are you really gonna take that food to it’s owner after it sat in the rain and now cold ?!
If it’s late drivers really need to ensure they have the correct home. I could not fall back to sleep after all that. I was soooo tired the next day. I even have a sign on my porch that says “ no trespassing “!
Get it together drivers!
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209


Various places throughout San Francisco.

The employer is not providing PPE for employees delivering to home and picking up from restaurants risking being infected with COVID-19.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-04-13 See Less
632


Didn’t get sick, and this happened months ago, but I ordered via DoorDash delivery and when it arrived found what looked like facial or pubic hair on the patty. Good thing I checked. Tossed it out and never ordered from this joint ever again! 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.

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.

Par is providing written notification to wholesale accounts and the hospital location that has received the affected lot and is arranging for the return of all existing inventory of Lot 57014 through Inmar, Inc. Wholesale distributors and hospital pharmacies that have the product being recalled should immediately discontinue the use and stop distribution immediately.

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

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-pharmaceutical-issues-voluntary-nationwide-recall-one-lot-treprostinil-injection-due-potential
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