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Covid-19 OSHA Complaint, Allure Pharmacy, 11670 San Vicente Boulevard, LOS ANGELES, CA, 90049, USA
2 years ago
11670 San Vicente Boulevard, Los Angeles, 90049 California, United States
1. T8 CCR § 3205(c) - In May 2021, the pharmacist/owner tested positive for COVID-19 and he did not wear any face coverings at work in dealing with customers and workers. 2. T8 CCR § 3362(a) - The toilet is very dirty, no regular cleaning. 3. T8 CCR § 3362(f) - There are roaches inside the bathroom.Alleged Hazards: 3, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-05-11
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Medline and Centurion Convenience kits - recalled due to lack of sterility, USA
2 weeks ago •source www.fda.gov
Recall notice
Water-based medical products that are non-sterile and potentially contaminated could cause serious or life-threatening infections, including bloodstream, urinary tract, open wound/soft tissue, and respiratory infections. Patients who are elderly, critically ill, have weak immune systems (including newborn infants, pregnant women, and cancer patients), or have chronic diseases are particularly at risk of infection. However, other patients could also develop infections after exposure to contaminated water-based medical products.
The recall affects Medline and Centurion convenience kits that may be used at home by patients, caregivers, and home health providers, as well as convenience kits that may be used in medical settings for surgery or other medical procedures. Recalled kits include, but are not limited to, wound care kits, tracheostomy kits and catheter kits. A detailed list of recalled Medline and Centurion convenience kits, as well as an example of product labeling, can be found in the link below.
Consumers who have recalled product should stop using the product and contact Medline immediately.
Medline Industries, LP notified its direct distributors and consumers of the Nurse Assist recall by First Class Mail and email on 11/16/23, upon receipt of initial recall notification from Nurse Assist. Customers who received the recalled product were given instructions to quarantine all affected products immediately and provide Medline with a response regarding the affected quantity on hand. Upon confirmation of the affected quantity, Medline provided customers with over-labels to place on the affected inventory, with instructions for staff to remove the affected component before using the kit. The recall notification also instructed distributors and those who resold or transferred affected product to another company or individuals to notify their customers of this recall notification.
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: Medline Industries, LP
Brand name: Medline and Centurion
Product recalled: Convenience kits
Reason of the recall: The potential for a lack of sterility
FDA Recall date: April 08, 2024
Source: www.fda.gov
Got a order of Keto+ACV Gummies/ I didn't order from DB, 192-01 Northern Boulevard, Flushing, NY 11354, USA
6 days ago •reported by user-hdmd4941
I recieve this bottle, McComb, MS, USA
1 week ago •reported by user-mzjwb374
A package I didn't order, Granbury, TX, USA
3 weeks ago •reported by user-rcjd6867
Unordered Package, Hamilton Township, NJ, USA
1 week ago •reported by user-zcwn4673
3 month wait for joggers, England, UK
6 days ago •reported by user-nwmyh313
AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence, USA
3 weeks ago •source www.fda.gov
Recall notice
Administration of an injectable product that contains particulate matter may result in local irritation or swelling. If the particulate matter reaches the blood vessels or is injected intravascularly 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. To date, Eugia US LLC has not received any reports of adverse events related to this recall.
Methocarbamol injection USP 1000 mg/10 mL (100mg/mL), is used as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. It is packaged in 10 mL and packed as 25 (vials) X 04 (Printed E-Flute cartons) X 01 (Shipper) with NDC code as 55150-223-10. Eugia US LLC shipped the entire lot to wholesalers nationwide from Jan 12, 2024, through Jan 16, 2024.
The product can be identified by product name on carton and vial label and with lot number 3MC23011 and Exp. Date: Nov 2026 (NDC 55150-223-10) (See enclosed vial label). The product label is as shown in the image below.
Eugia US LLC (f/k/a AuroMedics Pharma LLC) is notifying its distributors by recall letters and is arranging for the return/replacement of all recalled products. Wholesalers, hospitals, pharmacies, institutions, and doctors with an existing inventory of the recalled product lot should discontinue use, stop distribution and quarantine the product immediately. If you have further distributed the recalled product lot, notify your accounts and/or any additional locations which may have received the recalled product. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.
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.
If you are experiencing any harm after using this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Company name: Eugia US LLC
Brand name: Eugia US LLC
Product recalled: Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial)
Reason of the recall: Device & Drug Safety – Presence of Particulate Matter
FDA Recall date: March 28, 2024
Source: www.fda.gov
Foveth.com Judy Blues Scam, www.foveth.com
2 days ago •reported by user-hydjt464
I emailed them and they’re still claiming they shipped.
I bought four pairs of jeans $43 on March 8, 2024
I am reporting unordered package, Michigan, USA
1 week ago •reported by user-cghc2873
Heather Fottys
646 S Walcott Ave
Chicago IL. 60609
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