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Goodbye! and best wishes in your recovery

UnityPoint Health Methodist, 221 NE Glen Oak, PEORIA, IL, 61636, USA

Latest report: May 6, 2021 12:00 PM
RM

Covid-19 OSHA Complaint

2 years ago

1. Employees working in the Emergency Department are exposed to illnesses including coronavirus and the employer does not ensure the powered air purifying respirator filters are changed on a replacement cycle. 2. Employees are exposed to strains and crush-by injuries when moving bariatric beds with obese patients... See More and the employer does not ensure mechanical devices to move the patients or enough staff with procedures that will prevent injuries. 3. Employees working in the Emergency Department are exposed to punches, being choked and other assaults and the employer does not always investigate the instances and ensure security is used to control patients. Employees are exposed to psych patients and have not received crisis intervention training. 4. Employees are exposed to illnesses from blood and needles that were not cleaned from drawers and floors in the Emergency Department.

Alleged Hazards: 4, Employees Exposed: 25
Source: Osha.gov | Receipt Date: 2021-02-23
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283


EE

Covid-19 OSHA Complaint

3 years ago

Employees working in 8 Hamilton on the Adult Behavioral Health COVID-19 unit are exposed to SARS-CoV-2 and employees are not provided and required to use at least a N95 or higher level of respiratory protection.

Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-11-24 See Less
283


Related Reports

Covid number are spiking in the area, especially in the FedEx and UPS terminal, Missouri S&T and Rolla public school's. See Less
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Hospira, Inc., a Pfizer company, is voluntarily recalling 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10mL vial; 1% Lidocaine HCl Injection, USP, 50 mg/5mL vial; and 2% Lidocaine HCl Injection, USP, 100 mg/5mL vial to the user level due to the potential presence of glass particulate matter. To... See More date, Hospira, Inc. has not received reports of any adverse events associated with this issue for these lots. The products were distributed nationwide to wholesalers/hospitals/institutions in the United States and Puerto Rico from October 13, 2022 through October 26, 2022.

The recalled products are:
- 4.2% Sodium Bicarbonate Injection, USP Glass ABBOJECT® Syringe, NDC: Carton 0409-5534-24. Case: 0409-5534-14. Lot: GJ5007. Expiration Date: 1AUG2024. Presentation: 5 mEq/10mL, (0.5 mEq/mL) Configuration/ Count: 1 vial and injector/ carton 10 cartons/ bundle Case pack 5 X 10- 10mL
- 1% Lidocaine HCl Injection, USP LIFESHIELD® Glass ABBOJECT® Syringe. NDC: Carton 0409-4904-11 Case 0409-4904-34. Lot: 42290DK. Expiration Date: 1JUN2024. Presentation: 50 mg/5mL (10 mg/mL). Configuration/ Count: 1 vial and injector/ carton 10 cartons/ bundle Case pack 5 X 10- 5mL
- 2% Lidocaine HCl Injection, USP LIFESHIELD® Glass ABBOJECT® Syringe. NDC: Carton 0409-4903-11 Case 0409-4903-34. Lot: GH6567. ExpirationDate: 1JUL2024. Presentation: 100 mg/5mL (20 mg/mL). Configuration/ Count: 1 vial and injector/ carton 10 cartons/ bundle Case pack 5 X 10- 5mL

There is an unlikely probability for serious adverse events, including death, should a patient receive an injectable product found to contain particulate matter identified as glass. Potential complications related to injection of visible and subvisible inert particles include inflammation of a vein, granuloma, and blockage of blood vessels or life-threatening blood clot events. The frequency and severity of these adverse events could vary depending upon a variety of factors including the size and number of particles in the drug product, patient comorbidities (such as age, compromised organ function), and presence or absence of vascular anomalies. The risk is reduced by the possibility of detection, as the label contains a clear statement directing the healthcare professional to visually inspect the product for particulate matter and discoloration prior to administration.

Sodium Bicarbonate Injection, USP is a sterile, nonpyrogenic, hypertonic solution of sodium bicarbonate (NaHCO3) in water for injection for administration by the intravenous route as an electrolyte replenisher and systemic alkalizer. It is indicated in the treatment of metabolic acidosis which may occur in severe renal disease, uncontrolled diabetes, circulatory insufficiency due to shock or severe dehydration, extracorporeal circulation of blood, cardiac arrest and severe primary lactic acidosis. Sodium bicarbonate is further indicated in the treatment of certain drug intoxications, including barbiturates (where dissociation of the barbiturate-protein complex is desired), in poisoning by salicylates or methyl alcohol and in hemolytic reactions requiring alkalinization of the urine to diminish nephrotoxicity of hemoglobin and its breakdown products. It is also indicated in severe diarrhea which is often accompanied by a significant loss of bicarbonate.

Lidocaine Hydrochloride Injection, USP is a sterile, nonpyrogenic solution of an antiarrhythmic agent administered intravenously by either direct injection or continuous infusion. It is available in various concentrations. It is administered intravenously or intramuscularly and is specifically indicated in the acute management of ventricular arrhythmias such as those occurring in relation to acute myocardial infarction, or during cardiac manipulation, such as cardiac surgery.

Wholesalers, hospitals, institutions, and doctors with an existing inventory of a lot which is being recalled should discontinue use, stop distribution and quarantine the product immediately. If you have further distributed the recalled product, please 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.

Company name: Hospira, Inc.
Brand name: Hospira
Product recalled: 4.2% Sodium Bicarbonate Injection, USP, 1% Lidocaine HCl Injection, USP, and 2% Lidocaine HCl Injection, USP
Reason of the recall: Potential Presence of Glass Particulates
FDA Recall date: October 02, 2023

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-inc-issues-voluntary-nationwide-recall-42-sodium-bicarbonate-injection-usp-and-1-and-2
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We have been giving our dogs these treats, being advertised as a healthy alternative to raw hide. Our oldest female Chihuahua became ill on a Thursday evening. We contacted our vet and where advised to monitor her behavior and change her diet for twenty four hours. She... See More was vomiting and would not eat. Then diarrhea came. It was very bloody and had yellow in it with mucous. She was panting and trying to hide. The next morning her symptoms had become more severe. Our vet suggested we take her to an emergency hospital. Her kidney’s where failing and she was in diabetic shock. We where told with her age and symptoms she had a 5% chance to make it. She passed that morning. She was over 15 years old. She was part of our family. We trusted Dream Bones to be safe, do not be deceived!!! They are not safe and the FDA should start holding these companies accountable. There are no regulations on pet foods or treats! We should do better. Our furbabies deserve better standards. These bones poisoned all of our dogs and caused death in one. The company that markets these did treats need to be held accountable. Laws need to change and our pets need to be protected! | Symptoms: Diarrhea, Vomiting, Bloody Stool, Mucus in Stools See Less
6


My dog developed Inflammatory Bowel Disease after consuming Dream Bone products. His favorite treat was Dream Bone Sweat Potato bones. He would eat 1 to 2 bones daily. We have had to take him to the emergency vet twice for having a large amount of occult blood... See More in his stool. The emergency vet group (EVG) bills were close to $1000. | Symptoms: Bloody Stool See Less
669


Papa johns is not protecting their employees from COVID. I just got COVID and strep tested and it came back positive for both. They immediately told me to come back to work. This is completely unsanitary and unsafe for employees and customers. They are not following protocols... See More due COVID -19 and are disregarding everything just to have the correct amount of staffing. See Less
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Peoria Heights residents in 400-1000 blocks of Marietta, the 400-600 blocks of Moneta and Sciota, and the 4400 block of California are currently under a boil order, according to the Village of Peoria Heights website.

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I received a small white envelope in the mail. It contained a clear Iphone case. I did not order it See Less
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