Northern NJ Donor Center, 209 Fairfield Road, FAIRFIELD, NJ, 07004, USA
Latest report:
Covid-19 OSHA Complaint
2 years ago
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
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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
Source: Osha.gov | Receipt Date: 2021-02-05
747
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Hospira Sodium Bicarbonate & Lidocaine HCl Injections - recalled due to potential presence of glass particulate matter, USA
6 months ago •source www.fda.gov
Recall notice
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
…
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
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
303
Dream Bone dog treats, Jackson, KY, USA
6 months ago •reported by user-dhcr4146
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
…
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
6
My dog developing Inflammatory Bowel Disease after consuming a Dreambone daily, Needham, MA, USA
6 months ago •reported by user-hjgf9624
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
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in his stool. The emergency vet group (EVG) bills were close to $1000.
| Symptoms: Bloody Stool
669
Papa johns is not protecting their employees from COVID, Papa Johns Pizza, 9123 N Loop 1604 W, San Antonio, TX 78249, United States
8 months ago •reported by user-xwnh6111
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
…
due COVID -19 and are disregarding everything just to have the correct amount of staffing.
218
Power Outage, Villa Avenue, Fairfield, CT, USA
1 month ago
According to Fairfield Police, there is an incident in the 600 block of Villa Avenue after smoking wires on a utility pole. Power is out in the area according to media reports.
Outage link: outagemap.eversource.com/external/default.html
Source: www.doingitlocal.com/2024/03/fairfield-news-power-outage-19/
Published: 2024-03-11
Outage link: outagemap.eversource.com/external/default.html
Source: www.doingitlocal.com/2024/03/fairfield-news-power-outage-19/
Published: 2024-03-11
141
According to PG&E’s outage map, about 3,215 customers are affected by a power outage in Fairfield on Saturday afternoon, Mar 9. The affected area is near The Air Base Parkway. The outage started at 12:13 p.m. PST. The estimated time for restoration is listed at 3:45 p.m.
…
PST. Crews are working to restore power to the area. PG&E is investigating the cause of the outage.
Outage link: pgealerts.alerts.pge.com/outage-tools/outage-map/
Source: www.pge.com/en.html
Published: 2024-03-09
Outage link: pgealerts.alerts.pge.com/outage-tools/outage-map/
Source: www.pge.com/en.html
Published: 2024-03-09
120
Boil Water Advisory, County Road 1800, Fairfield, IL, USA
1 month ago •reported by user-vmqk1986
New Hope Water customers in the area of County Road 1800 East from County Highway 8 to 200 North and West of 1800 East are under a boil order until further notice. The order is due to a water line that had been hit.
Source: www.wfiwradio.com/2024/03/06/new-hope-boil-order/
Published: …
Source: www.wfiwradio.com/2024/03/06/new-hope-boil-order/
Published: …
2024-03-06
2
According to PG&E’s outage map, a power outage is affecting customers in the Travis Air Force Base neighborhood in Fairfield, on Thursday afternoon, Feb 8. About 12,654 customers are currently impacted. The outage is impacting also Rio Vista. The outage started today at 6:24 a.m. The estimated
…
time for restoration is to be determined. The outage was caused by the weather. Crews are working to restore power to the area.
Outage link: pgealerts.alerts.pge.com/outage-tools/outage-map/
Source: www.pge.com/en.html
Published: 2024-02-08
Outage link: pgealerts.alerts.pge.com/outage-tools/outage-map/
Source: www.pge.com/en.html
Published: 2024-02-08
2
Power Outage, North Benson Road, Fairfield, CT, USA
2 months ago
A power outage has been reported affecting Fairfield University's North Benson Campus and surrounding areas after a United Illuminating transformer outage on North Benson Road. According to the outage map, power has been restored.
Outage link: www.uinet.com/outages/reportviewoutage/viewoutagemap
Source: connecticut.news12.com/ui-transformer-outage-leaves-fairfield-university-north-benson-campus-without-power
Published: 2024-01-30
Outage link: www.uinet.com/outages/reportviewoutage/viewoutagemap
Source: connecticut.news12.com/ui-transformer-outage-leaves-fairfield-university-north-benson-campus-without-power
Published: 2024-01-30
141
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received by Logistic  895 Meyerside Dr MISSISSIGA ONTARIO CANADA. JY243510U16208****
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I ordered a bra. It doesn’t fit. I need to send it back. There is no paper work . And I don’t know who to talk to.
2
D
user-dqfx6869
I got a package just like this it when attached to two different TV’s othi g happened, I was y my money back..
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- Reply
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