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Bubba Gump Shrimp Co.
Updated: July 14, 2020 12:51 PM
I was Rushed to the hospital for a bad allergic reaction, Bubba Gump Shrimp Co., Las Vegas Boulevard South, Las Vegas, NV, USA
Symptoms: Diarrhea Nausea Vomiting Other
Bubba Gump Shrimp Co., Las Vegas Boulevard South, Las Vegas, NV, USA
July 14, 2020 12:51 PM
“I was Rushed to the hospital for a bad allergic reaction & they refuse to refund.
They were informed of my food allergies before ordering. They messed up my order twice and informed me that there was no tomatoes or jalapeños peppers in the remade dishes but I still had an allergic reaction to th... e food. No could tell me if the dish was prepared separate, with clean, uncontaminated utensils. If the cook changed his gloves before pairing my food or if he'd touch tomatoes or jalapeños when preparing my dish or card to answer any of my questions. The response was, "well we made a knew dish. I don't know what happened." No one took responsibility.
The the staff were not trained to respond in a food allergy emergency. My tongue, lips and throat swelled. The waiter gave me water and ice, I took benadryl, then began vomiting the contaminated food. My friend and another customer had to get help and tell the manager to call 911. The manager comped one dish and made My friend pay the bill before the ambulance took me to the hospital.
This is unacceptable & I could've died because of the neglect and care with the food and on my birthday vacation. This was a horrible experience. Allergic reaction to the food. ”
Doctor Visit: Yes
Diagnosis: Urgent Care
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Fresenius Kabi USA Ketorolac Tromethamine Injection, USP, 30 mg/mL - recalled due to Presence of particulate matter, USA
January 8, 2021 6:01 PM
“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketoro... lac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter. Particulate matter was found in reserve sample vials. No adverse event reports have been received for the recalled lot, which was produced and sold in 2019.
Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.
Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine Injection should not exceed 5 days. Listed below is a table of the recalled lot distributed nationwide in the United States to wholesalers, distributors, hospitals, and pharmacies between March 28, 2019 and September 3, 2019.
Product Name/Product size: Ketorolac Tromethamine Injection, USP, 30mg / mL, 1 mL fill in a 2 mL amber vial
NDC Number: 63323-162-01
Product Code: 160201
Batch Number: 6121083
Expiration Date: 02/2021
First Ship Date: 03/28/2019
Last Ship Date: 09/03/2019
Fresenius Kabi is notifying its distributors and customers by letter and asking customers and distributors to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product. Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing the affected lot, and to return the product to Fresenius Kabi.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA ”
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