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HCA Healthcare, One Park Plaza, NASHVILLE, TN, 37203, USA

Total all time reports:  1
Latest report: May 5, 2021 12:00 PM

Covid-19 OSHA Complaint

May 5, 2021 12:00 PM

“Location: HCA-Affiliated Kendall Regional Medical Center in Miami, Florida 1)Employees are being supplied with KN-95's that are not NIOSH-certified respirators for use when providing health services to patients who are COVID-19 positive, a possible violation of 29 CFR 1910.134. 2) The employees have... See Morenot received respirators when needed because the respirators are being stored under lock and key; a possible violation of 29 CFR 1910.134. 3) The employees have not received hair or shoe protection, and adequate amounts of disposable isolation gowns; a possible violation of 29 CFR 1910.132. 4) Staff routinely brings PPE from home due to lack of enough or correct PPE to protect themselves and their patients; a possible violation of 29 CFR 1910.132. 5) The hospital has not used negative airflow rooms with HEPA filtration systems when needed; a possible violation of the OSH Act 5(a)(1) general duty clause. 6) The hospital has not established transporting procedures of COVID-19 patients, exposing employees to possibly contracting SARS-CoV-2 and/or COVID-19; possible violation of the OSH Act 5(a)(1) general duty clause. Location: HCA-Affiliated Northwest Medical Center in Margate, Florida 1) Employees are being supplied with KN-95's that are not NIOSH-certified respirators for use when providing health services to patients who are COVID-19 positive, a possible violation of 29 CFR 1910.134. 2) The employees have not received respirators when needed because the respirators are being stored under lock and key in the fourth (4th) floor hub room that closes at 10:00pm ; a possible violation of 29 CFR 1910.134. 3) The employees have not received hair or shoe protection, and adequate amounts of disposable isolation gowns; a possible violation of 29 CFR 1910.132. 4) Staff routinely brings PPE from home due to lack of enough or correct PPE to protect themselves and their patients; a possible violation of 29 CFR 1910.132. 5) The hospital has not used negative airflow rooms with HEPA filtration systems when needed; a possible violation of the OSH Act 5(a)(1) general duty clause. 6) The hospital has not established transporting procedures of COVID-19 patients, exposing employees to possibly contracting SARS-CoV-2 and/or COVID-19; possible violation of the OSH Act 5(a)(1) general duty clause. Location: HCA-Affiliated Plantation General Hospital in Plantation, Florida 1) Employees are not provided sufficient personal protective equipment (PPE); a possible violation of 29 CFR 1910.132. 2) Employees respirators are being placed in paper bags, but procedures for re-use and/or cleaning of respirators are not being provided; a possible violation of 29 CFR 1910.134. Location: HCA-Affiliated Palms West Hospital in Loxahatchee, Florida 1) Employees are not provided with N-95's or an equivalent respirator when providing health services to patients who are COVID-19 positive, a possible violation of 29 CFR 1910.134. 2) The employer has given inconsistent instructions on the extended use of N-95 respirators, a possible violation of 29 CFR 1910.134. 3) The employees have not received hair or shoe protection, and adequate amounts of disposable isolation gowns; a possible violation of 29 CFR 1910.132. 4) Staff routinely brings PPE from home due to lack of enough or correct PPE to protect themselves and their patients; a possible violation of 29 CFR 1910.132. 5) The Employees have been exposed to workplace violence while performing normal duties with patients; a possible violation of the OSH Act 5(a)(1) general duty clause. Location: HCA-Affiliated St. Lucie Medical Center in Port St. Lucie, Florida 1) The employees do not have access to respirators when needed, due to the lack of respirators available; a possible violation of CRF 29 1910.134. 2) EVS is not cleaning the surgery rooms and cleaning materials are not available to the surgery staff, a possible violation of 29 CFR 1910.1030. 3) Employees respirato


Source: Osha.gov | Receipt Date: 2020-06-26
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Reported By SafelyHQ.com User

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Recall details: Dash Xclusive is voluntarily recalling all lots of Imperia Elita Vitaccino Coffee to... See Morethe consumer level. FDA analysis has found the product to contain undeclared sibutramine and fluoxetine. Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues, including stroke, heart failure and serious health risk especially to those with underlying heart related disease.

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Risk Statement: Products containing undeclared sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.

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The product is marketed as a dietary supplement for weight loss and is packaged in a black rectangular box and contains fifteen sachets. The affected Imperia Elita Vitaccino coffee lots include all lots. Product was distributed Nationwide in the USA via internet and by ebay at www.ebay.com.

On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms. Dash Xclusive is notifying its customers by e-messages on the eBay platform and is arranging for return of all recalled products. Consumers that have Imperia Elita Vitaccino Coffee which is being recalled should stop using/return to Dash Xclusive, PO BOX. #220, 1125 E. Broadway Glendale, California 91205.

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. 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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Methanol was discovered through lab testing. To date, Global Sanitizers has not received any reports of adverse events related to this recall. We began shipping this product on approximately July 10, 2020. Immediately examine your inventory and quarantine product subject to recall.

In addition, if you may have further distributed this product, please identify your customers and notify them at once of this product recall. Your notification to your customers may be enhanced by including a copy of this recall notification letter.

If you have these recalled items in stock, please send an email to recall@globalsanitizers.com and we provide further instructions for product destruction. This recall should be carried out at the consumer level. This recall is being made with the knowledge of the Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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“Company name: Sanit Technologies LLC d/b/a Durisan
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In the April 10, 2021 announcement, Durisan expanded the recall to include all of its Hand Sanitizer products that had not expired (produced after 4/10/2019). Durisan discovered that promotional orders, as well as small run production lot numbers which were not listed, were intended for inclusion in the recall. For clarification, in the link below are all affected lot numbers.

Customers or consumers in possession of Durisan Non Alcohol Antimicrobial Hand Sanitizer products with these numbers in any form factor are encouraged to contact Durisan. To date, no qualified reports of adverse reactions have been reported related to this recall. The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available.

The product is packaged in sizes ranging from 18mL credit cards, to bottles sized in 118, 236, 300 and 550 mL and 1000mL wall mounted dispenser refills. At this time, we are including lot numbers of promotional orders, wipes, and private label products. The lot number can be found in black print on the bottom of the package. Durisan Antimicrobial Solutions hand sanitizer sizes with the identification are listed in the link below.

Durisan has provided written notification to its distributors and retailers and is alerting consumers via this voluntary recall. Consumers that have the product are advised to contact Durisan to return it. 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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May 19, 2021 1:00 PM

“Company name: Dibar Nutricional S. de R.L. de C.V.
Brand name: DIBAR Labs, ProtectoRx
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 19, 2021
Recall details: Morelia, Michoacán, Mexico, Dibar Nutricional S. de R.L. De C.V. (“Dibar”) is voluntari... See Morely recalling all Dibar Labs Hand Sanitizer packaged in 8oz and 16 oz bottles, respectively, to the consumer level (see Label 1 below). Dibar is also voluntarily recalling ProtectoRx Hand Sanitizer packaged in 2oz and 16oz fluid ounce bottles, respectively, to the consumer level (see Label 2 below), as well as all Advance Hand Sanitizer packaged in 16 oz bottles, likewise, to the consumer level (see Label 3 below). These products are being recalled after testing conducted by our firm revealed the presence of methanol.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning.

To date, the company has not received any reports of adverse reactions related to this recall. These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available.

The affected bottles of hand sanitizer include a twelvedigit lot code printed on the bottle near the base. The products can be identified by the label image provided at the end of this release. Products labeled as Dibar Labs Hand Sanitizer were distributed nationwide in the USA through S.E.N.D. LLC and its customers. Products labeled as ProtectoRx Hand Sanitizer were distributed in Puerto Rico through PR TRADING LLC and its customers. Products labeled as Advance Hand Sanitizer were distributed in the USA through RGV HEALTH SERVICES LLC DBA VALLEY and its customers.

Dibar Nutricional S. de R.L. De C.V., has notified its direct distributors by letter and asked that they remove the recalled products from commerce immediately if they still possess inventory.

Consumers, distributors and retailers that have the hand sanitizers which are being recalled should stop using, distributing and/or selling them and return them to the place of purchase. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online by regular mail or by fax.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Link to Original Recall

Check the full recall details on fda.gov

Source: FDA
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