ORA Space, 9 E 4th St., NEW YORK, NY, 10003, USA
Latest report:
Covid-19 OSHA Complaint
2 years ago
1) The employer has not implemented and develop a blood borne pathogen program for the workplace where employee have an exposure to sharps (i.e., acupuncture needles). 2) The employer did not ensure that sharp containers are changed in a timely manner to prevent acupuncture needles from over
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flowing out of the container. 3) The employer did not train employees on the proper disposal of acupuncture needles. The needles when placed in the container are sticking out. 4) The employer did not ensure that the sharps container are the proper size to hold the acupuncture needles and are in compliance with regulations.
Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-02-10
Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-02-10
2.8K
Related Reports
Covid cases in my area are high, Rolla, MO, USA
4 months ago •reported by user-cvttz511
Covid number are spiking in the area, especially in the FedEx and UPS terminal, Missouri S&T and Rolla public school's.
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user-tnvv1773
costco optical lab employees are using and selling drugs in the lab
- 1 month ago
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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
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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
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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
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due COVID -19 and are disregarding everything just to have the correct amount of staffing.
218
They do not perform as advertised, West 56th Street, New York, NY, USA
3 days ago •reported by user-jbtr1945
I was supposed to receive three pairs of the adjustable glass; however, I received six pairs. Furthermore they do not work as advertised. I want to return them.
Received 6 pairs rather than 3. They do not perform as advertised. I wish to return them.
Received 6 pairs rather than 3. They do not perform as advertised. I wish to return them.
2.8K
Fake ring sent, New York, NY, USA
4 days ago •reported by user-hpwcr899
Bought two ser of items feom Fashion Nova and I received a fake ring
2.8K
Online Scam, New York City, NY, USA
4 days ago •reported by user-zdvm8952
I am reporting watt I think is definitely a scam from tradejilong. com took my money provide me with a fake tracking number and I've been waiting 17 days as it says it would take to get here been watching the item from China until it gets
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to Cincinnati Ohi. Tradejilong. com is a scamming sight so people please don't even think about shopping from them
2.8K
Scam, NYC, NY, USA
1 week ago •reported by user-kggw2784
Is your facility a distributor for an overseas market? I received a bracelet I didn’t order and didn’t get 2 bag charms I did order from HGate. Already opened a dispute with them .
2.8K
I am reporting a bottle of subgenix, New York, NY 10024, USA
1 week ago •reported by user-dfhq9323
I received a package that I did not order. A bottle of subgenix bioribose.
1.0K
Recent Interesting Reports
I have been receiving packages from this company that I did not order., Las Vegas, NV, USA
3 weeks ago •reported by user-pmmkg943
Don’t send any more of these Speedy gummies AGC Return my money.
The last two pack ages of 5 bottles each I have refused.. The address is PO Box 81559 from Las Vegas, NV 89189 package is in grey wrapping and I have not opened it. It is from Speedy
The last two pack ages of 5 bottles each I have refused.. The address is PO Box 81559 from Las Vegas, NV 89189 package is in grey wrapping and I have not opened it. It is from Speedy
1.4K
Not the same as advertised, New Orleans, LA, USA
1 day ago •reported by user-ybpyc327
I order two of the nano tech bullet proof vest, when it arrived the material was a thin allistic material and not seeing hours this material could stop any for arm nor knife stabbing.. I want the correct item or my money back!! But it came from Heathers Morty’s out of Union City, New Jersey 07087
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Same thing, Dallas, TX, USA
4 days ago •reported by user-vcjnp739
I placed a order on March 12th from the same company and got a tracking number stayed watching it as it supposedly went to each destination till it stated delivered on March 27th. But nothing came, my husband stayed my the front door all day waiting for
…
it, for nothing to arrive. I've reached out to customer service with no success to do anything. And im out of $150 of my hard working money just gone...... I'm so upset don't know who to turn to. The website stated they were affiliated with Amazon and it was a secured site so I believed it was ok...... how can they use a logo of such magnitude and not be real???
786
Not ordered products, Tampa, FL 33675, USA
4 weeks ago •reported by user-bknwr732
I got this shit in the mail and through local law enforcement officials investigating a fraudulent transaction case, you were determined to be the thief. Where do you want this shit sent from here you thief?
This package arrived addressed to me, I opened it and found …
This package arrived addressed to me, I opened it and found …
the product inside that I never ordered. I don’t want it and refuse to pay for something I didn’t order. What should I do with it?
USPS tracking number 9400111206217603******. There has been a investigation started by the the one police Department and fraud charges are being charged against your company for stealing money for my social security pay for this product.
Im in Des Moines, IA, USA
USPS tracking number 9400111206217603******. There has been a investigation started by the the one police Department and fraud charges are being charged against your company for stealing money for my social security pay for this product.
Im in Des Moines, IA, USA
523
I ordered a Stealth Bird Drone online what I got is not what I ordered., Tech 1 (US) 192-01 Northern Blvd, Flushing, NY 11358, USA
3 days ago •reported by user-xwzqn837
This business or person advertised a Steath Bird 4K Drone online for $99.00 plus free shipping. I received an older model Drone, and possibly used. No, business name no,phone number to call. I feel I got scamed.
1.4K
USPS Teterboro Distribution Center - the Bermuda Triangle of postal deliveries, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
1 week ago •reported by user-cmzg5894
Had an item shipped on 3/18/24 from MA to my home in NJ. It's been stuck in Teterboro for a week and a half. Either it was stolen or lost. Neither of which is acceptable. I was actually told by two different postal employees there is a
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HUGE theft issue at that location. This is why UPS and FedEx are both doing a bang up business. Meanwhile, the state and federal governments expect us to have trust when we use absentee ballots for elections. What a total joke.
#uspostalservice #200industrialavenue #teterboro #newjersey #us #usps
#uspostalservice #200industrialavenue #teterboro #newjersey #us #usps
1.0K
D
user-dpnfg765
did your item ever arrive? I mailed a package to NJ and no updates since it arrived in Teterboro on 04/01.....
- 3 days ago
- Reply
Unordered Ring, Knoxville, TN, USA
3 weeks ago •reported by user-pgjkw527
I received a ring from second brother NY I DID NOT ORDER
249
Scam, unable to contact anyone to cancel order, Novi, MI, USA
2 days ago •reported by user-jwwtf638
I have been trying to cancel my order and there is nowhere to do so.
251
Walmart Mainstays Electric Mini Choppers recalled due to Laceration Hazard, USA
1 week ago •source www.cpsc.gov
Recall notice
Walmart has issued a recall for over 51,750 units of its Mainstays Electric Mini Choppers due to a laceration hazard. The product, sold exclusively at Walmart, has a blade that can operate unexpectedly, posing a risk to consumers. The issue came to light after Walmart received five
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reports of lacerations, two of which required medical attention, including stitches. These injuries occurred during assembly or cleaning/handling of the product.
The choppers were sold at Walmart stores nationwide and online from August 2022 through October 2023, priced between $10 and $15. The recalled product is the Mainstays Electric Mini Chopper with model number MS14100094536S1. These choppers are rechargeable and cordless, featuring a green lid, white body, and clear plastic bowl. They come with a single blade attachment, which includes three curved blades on a white plastic spindle. The model number can be found on the label attached to the bottom of the clear plastic bowl.
Consumers should immediately stop using the recalled choppers, and contact Walmart to receive a full refund. Consumers can bring the chopper to their nearest Walmart store for a refund.
If you or a loved one are harmed, it is important to report it. Reporting can help to detect & resolve issues early and prevent others from being harmed, and enables better surveillance. If symptoms persist, seek medical care.
Source: www.cpsc.gov/Recalls/2024/Walmart-Recalls-Mainstays-Electric-Mini-Choppers-Due-to-Laceration-Hazard-Sold-Exclusively-at-Walmart
The choppers were sold at Walmart stores nationwide and online from August 2022 through October 2023, priced between $10 and $15. The recalled product is the Mainstays Electric Mini Chopper with model number MS14100094536S1. These choppers are rechargeable and cordless, featuring a green lid, white body, and clear plastic bowl. They come with a single blade attachment, which includes three curved blades on a white plastic spindle. The model number can be found on the label attached to the bottom of the clear plastic bowl.
Consumers should immediately stop using the recalled choppers, and contact Walmart to receive a full refund. Consumers can bring the chopper to their nearest Walmart store for a refund.
If you or a loved one are harmed, it is important to report it. Reporting can help to detect & resolve issues early and prevent others from being harmed, and enables better surveillance. If symptoms persist, seek medical care.
Source: www.cpsc.gov/Recalls/2024/Walmart-Recalls-Mainstays-Electric-Mini-Choppers-Due-to-Laceration-Hazard-Sold-Exclusively-at-Walmart
303
Gummies - Fraudulent order, 192-01 Northern Boulevard, Flushing, NY, USA
6 days ago •reported by user-qvmpn268
I received gummies I did not order. I don't want to be charged.
1.4K
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