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Updated: June 13, 2021 12:00 PM
1 year ago
1. Employees are not enforced to wear masks and gloves during covid 19 pandemic. 2. The store lobby is open, but the area isn't being sanitized or disinfected properly. 3. Employees who have been exposed are not required to self-quarantine. 4. Management is not telling employees of... potential exposure to coronavirus.
Source: Osha.gov | Receipt Date: 2020-05-21
1 year ago
1. The employer is not following the Governor's directives for COVID-19. Cleaning and disinfecting of high touch surfaces is not conducted as required. 2. Employees who have direct exposure to COVID are still allowed to work. 3. Employees are not being allowed to take off work to... have a COVID test conducted. They are told that if they do not come into work that they will be fired. HAZARD LOCATION: Throughout 11/16/2020 KR
Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-11-10
T8CCR 3362(f) Roaches & rats. T8CCR 3380(a) No gloves provided to employees. T8CCR 3362(a) No sanitation supplies provided to employees to clean properly and prevent vermin. T8CCR 3203(a) Employer did not take action when employee reported had caught Covid.
Alleged Hazards: 4, Employees Exposed: 13
Source: Osha.gov... | Receipt Date: 2020-10-12
1 year ago
Multiple employees(2) at DEL TACO in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 11/11/2020,
#coronaviruscovid19 #deltaco #4720montgomeryboulevardnortheast #albuquerque #newmexico #unitedstates #taco
2 years ago
T8 CCR 3203(a)(4) Employer is not providing adequate personal protective equipment, such gloves, employees use the same gloves for hours, no sanitizer, minimal hand washing.
Alleged Hazards: 1, Employees Exposed: 13
Source: Osha.gov | Receipt Date: 2020-07-13
2 years ago
1. The employer is not following the Governor's COVID-19 Guidance as customers are not required to wear face masks within the establishment. Employees are concerned for their health.
Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-06-26
I contacted the manager at your store because my sister consumed an undercooked burger last night and is now very sick. He said that there was no way she can get sick from beef even though a quick google search says otherwise. I’m very disappointed.
#deltaco #undercooked #foodsafetyissue #4418hamiltonroad #columbus #georgia #unitedstates #burger #beef
Recent Interesting Reports
3 days ago
Yesterday(not positive about the time. My guess; 6 p.m.) I heard a very large "BANG", like there was an accident and someone hit the area where my power rights are located. The power went out immediately. I walked outside earlier this a.m. I see no lights on... at my neighbor's homes on my side of the street.i see lights on across the street. I see lights on outside where the new apartments are being built next door to my house on the same side of the street. Do you know when our power will be back on. My freezer items are defrosting now. CAN YOU PLEASE LET ME KNOW THE STAUS AND WHEN YOU THINK OUR POWER WILL BE BACK ON PLEASE? I DO NOT FEEL AS SAFE AS I SHOULD FEEL. THIS IS NOT A GOOD FEELING AT ALL!
1 day ago
This company has alot of violations they work without gloves. They also sell rotten crabs and fish to people who buy. They don’t throw anything away. The old stuff like rice with mouth poop and Rouches they mix with new ones and sell it. They leave the... fish out in the heat. They have a mouse and rouches problem big time. They have no Ventilations for the food or Meats. They have under age people working and Undocumented. Please send someone thats going to do the Job right in not get paid in leave.Thanks please send someone as soon as possible
Supplement - captain boss bully ruby 10000 made my eyes burn,water, skin burn, vomiting, shaking, goosebumps. One of the worst experiences of my life, Glenmont, NY, USA
2 weeks ago
A supplement called captain boss bully ruby 10000 made my eyes burn,water,skin burn, vomiting, shaking, goosebumps. One of the worst experiences of my life
I bought it at a convenience store witch was prob my first mistake. I’ve taken them before and never had any issues. It... was the only brand left so I have it a go 20 minutes later my fave and eyes started burning and my eyes got really red. I got home around 830 took a shower and no longer then 5 min started puking none stop. It’s been going on for 3 hrs. Dizzy, goosebumps and worst of all I’m not in the mood whatsoever now. | Symptoms: Vomiting, Shaking
Golden State Medical Supply, Incorporated (GSMS, Inc.) - Camarillo, CA has initiated a voluntary recall of the products listed in the table below because a report was received that a bottle containing Clopidogrel 75mg Tablets produced with lot# GS046745 was mislabeled as Atenolol 25mg Tablets. This voluntary... recall only affects products with lot# GS046745. No other Clopidogrel or Atenolol products marketed by GSMS, Inc. are impacted. Both products are being recalled out of abundance of caution.
Product Description: Clopidogrel 75mg Tablets, 1,000 Count Bottle, GSMS NDC: 51407-032-10, Lot #: GS046745, Expiration Date: 12/2023
Product Description: Atenolol 25mg Tablets, 1,000 Count Bottle, GSMS NDC: 60429-027-10, Lot #: GS046745, Expiration Date: 12/2023
Atenolol tablets are indicated for the treatment of hypertension, to lower blood pressure. Clopidogrel is prescribed to lower the risk of having a stroke, blood clot, or serious heart problem for patients who have had heart attack, severe chest pain, or circulation problems as indicated in the product labeling. For more drug label information about clopidogrel bisulfate visit: DailyMed - CLOPIDOGREL- clopidogrel bisulfate tablet, film coated (nih.gov). For more drug label information about atenolol visit: DailyMed - ATENOLOL tablet (nih.gov)
Patients who suddenly stop taking atenolol, as would happen if clopidogrel were misplaced in the atenolol-labeled bottle, are at increased risk for ischemic (angina, myocardial infarction), hypertensive and arrhythmic adverse events relating to rapid withdrawal of beta antagonism. Further, patients who are on atenolol are frequently on concomitant anticoagulant and antiplatelet medications and would be at increased risk for bleeding if clopidogrel were added to the regimen. To date, GSMS, Inc. has not received any reports of adverse events related to the use of the products as part of this recall.
The lot under GSMS, Inc.’s voluntary recall has been primarily sold to AmerisourceBergen, and McKesson. AmerisourceBergen and McKesson are instructed to immediately stop distribution, quarantine all remaining products in their control, and return the recalled product to GSMS, Inc. They are also instructed to provide their customers, i.e., pharmacies and consumers, a copy of GSMS, Inc.’s recall notification, recall response form, and letter to consumers, patients, and caregivers.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
In case you experienced harm from these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.
Company name: Golden State Medical Supply, Incorporated
Brand name: Golden State Medical Supply, Incorporated
Product recalled: Clopidogrel 75mg Tablets, Atenolol 25mg Tablets
Reason of the recall: Due to Label Mix-up
FDA Recall date: September 29, 2022
From 23rd Ave SW to 22nd Ave SW there is no electricity??? Why is there one in its surroundings, 4961 23rd Avenue Southwest, Naples, Florida, USA
1 day ago
Two streets from 23rd Ave to 22nd Ave
Is there no electrical power????
And if adjoining streets
Philips Respironics CPAP or Bi-Level PAP therapy masks - recalled due to potential risk of serious injury, USA
3 weeks ago
These masks may continue to be used according to the updated instructions and labeling if patients or people in close proximity to them do not have implanted metallic medical devices or metallic objects in the body.
Royal Philips’ (NYSE: PHG; AEX: PHIA) subsidiary Philips Respironics is alerting... users of certain CPAP or Bi-Level PAP therapy masks with magnetic headgear clips or straps that these devices should not be used by or near patients and their household members, caregivers and bed partners who have metallic implanted devices or metallic objects (such as metallic splinters) in the body. The magnetic headgear clips are used to attach the headgear straps to the masks, which is a method that is commonly used in the sleep therapy devices industry.
This is a voluntary notification to users of specific CPAP or Bi-Level PAP therapy masks containing such magnetic clips to inform them of the updated instructions and labeling. All users should read and follow Philips Respironics’ voluntarily updated warning and added contraindication described below. This represents a new and industry-leading practice.
Contraindication: Use of the mask is contraindicated for patients and their household members, caregivers and bed partners that may be in close vicinity to patients using the masks, that have implanted devices that may be affected by magnets, including but not limited to:
- Implantable cardioverter defibrillators (ICD)
- Magnetic metallic implants/electrodes/valves placed in upper limbs, torso, or higher (i.e., neck and head)
- Cerebral spinal fluid (CSF) shunts (e.g., ventriculo peritoneal (VP) shunt)
- Aneurysm clips
- Embolic coils
- Intracranial aneurysm intravascular flow disruption devices
- Metallic cranial plates, screws, burr hole covers, and bone substitute devices
- Metallic splinters in the eye
- Ocular implants (e.g., glaucoma implants, retinal implants)
- Certain contact lenses with metal
- Implants to restore hearing or balance that have an implanted magnet (such as cochlear implants, implanted bone conduction hearing devices, and auditory brainstem implants)
- Magnetic denture attachments
- Metallic gastrointestinal clips
- Metallic stents (e.g., aneurysm, coronary, tracheobronchial, biliary)
- Implantable ports and pumps (e.g., insulin pumps)
- Hypoglossal nerve stimulators
- Devices labeled as MR (Magnetic Resonance) unsafe
- Magnetic metallic implants not labeled for MR or not evaluated for safety in a magnetic field
Patients should stop using the affected mask if the implant/medical device is contraindicated against the mask magnets. Patients should consult their physician immediately to determine if another mask can be used for their therapy. In the interim, switch to a non-magnetic mask if available, for continued therapy.
Patients should properly dispose of the mask that has magnets after an alternative is obtained. These masks may continue to be used according to the updated instructions and labeling if patients or people in close proximity to them do not have implanted metallic medical devices or metallic objects in the body.
Warning: Magnets with a magnetic field strength of 400 mT are used in the mask. With the exception of the devices identified in the contraindication, ensure that the mask is kept at least 6 inches (approx. 15 cm) away from any other medical implants or medical devices that can be impacted by the magnetic fields to avoid possible effects from localized magnetic fields. This includes household members, caregivers, and bed partners that may be in close vicinity to patients that use the masks.
Impacted masks include: More than 17 million masks containing magnetic clips have been distributed by Philips Respironics to date. As of August 30, 2022, Philips Respironics has received 14 reports of patients suggesting that the mask magnets may have impacted their medical devices including pacemaker interference, pacemaker failure leading to replacement, need of shunt adjustment, resetting of automatic implantable cardioverter defibrillator (AICD), seizures, defibrillator shutting off periodically, arrhythmia, irregular blood pressure, change in heartbeats, and cognitive issues.
Patients may contact their Durable Medical Equipment (DME) provider, which supplied the masks affected by this notice. This voluntary medical device corrective action has been reported to the regulatory agencies in the countries where these masks are available.
In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.
Company name: Royal Philips’ subsidiary Philips Respironics
Brand name: Philips
Product recalled: Certain CPAP or Bi-Level PAP therapy masks with magnetic headgear clips or straps
Reason of the recall: potential risk of serious injury
I receive an empty envelope USPS TRACKING #
9400 1362 0633 5670 0
I'm in Sarasota, FL, USA
Lake Byllesby beach in Cannon Falls, MN closed due to E. coli, Lake Byllesby Beach, Echo Point Rd, Cannon Falls, MN 55009, USA
4 weeks ago
Lake Byllesby beach has been closed until further notice by Dakota County due to high E. coli levels. Beach water testing will resume on Tuesday, Sept. 6 when the lab reopens. Dakota County will notify the public when E.coli levels are safe for beach visitors.
Received an empty package - from 188 South Mountain house Parkway Tracy CA 95377, 188 South Mountain House Parkway, Tracy, CA, USA
4 days ago
Although I received an empty package from 188 South Mountain house Parkway Tracy CA 95377 the 1st class postage says mailed from zip 90021 on September 24, 2022.
#onlineshopping #emptypackage #amazon #delivery #uspostalservice #188southmountainhouseparkway #tracy #california #unitedstates
Last 30 days