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Covid-19 OSHA Complaint, Northern NJ Donor Center, 209 Fairfield Road, FAIRFIELD, NJ, 07004, USA

2 years ago

209 Fairfield Road, Fairfield, 07004 New Jersey, United States

1. Employees are suffering from musculoskeletal disorders due to loading and unloading blood collection equipment from the trucks and also with assisting patients on and off the tables. 2. Employees have not received adequate ergonomic training. 3. Employees utilized chemical to clean equipment and patient collection tables have not received adequate training. 4. Employees have received needle sticks from equipment used in blood draws. 5. Employer has not performed a hazard assessment for employee exposed to patient to determine COVID exposure. 6. Employer has not provided proper PPE and training to employee for COVID exposure. 7. Employer is not properly recording COVID illness in the OSHA 300 logs. 8. Employee is not following CDC guidelines related to COVID precautions such as not being able to socially distance and are working in unventilated indoor spaces. 9. Employees are not being notified when they are exposed to donors/coworkers under investigation for COVID. 10. Employer is not ensuring that contracted cleaning services are properly disinfecting the worksites per the CDC guidelines.


Source: Osha.gov | Receipt Date: 2021-02-05

747


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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.

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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

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