Little Caesars Pizza, 725 28th St SW, Wyoming, Michigan 49509, USA
Latest report:
Covid-19 OSHA Complaint
3 years ago
1. The employer recently wasn?t providing face masks nor requiring that employees wear one during the COVID-19 pandemic.
2. The employer is charging the employees for masks.
Source: Osha.gov | Receipt Date: 2020-07-09
2. The employer is charging the employees for masks.
Source: Osha.gov | Receipt Date: 2020-07-09
296
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.
92
T
user-tnvv1773
costco optical lab employees are using and selling drugs in the lab
- 1 month ago
- Reply
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
Floor Cracks Walls etc., SWF1 Amazon, 635 International Blvd, Rock Tavern, NY, USA
10 months ago •reported by user-fyyym648
Floor cracks are getting wider and destroying our PIT equipment, walls are uneven and mold is at an all time high as employees struggle to breathe comfortably in the warehouse. Mold in floor cracks and between walls and boxes. Low quality concrete floor unsafe to support 6 ton PIT.
90
Possible COVID-19 Symptoms, Cook Out, West Cumberland Street, Dunn, NC, USA
1 year ago •reported by user-rdqk1975
I started feeling symptoms yesterday morning after eating at this location in Dunn. The location was very dirty and none of the people wore masks. I have had to cancel my driver's test, dentist appointment, doctor's appointment and several other events.
| Symptoms: Other
13
Lockport CARES, Lockport CARES, Inc, Genesee Street, Lockport, NY, USA
1 year ago •reported by user-fmqy4141
I was staying at a shelter in Lockport Cares and there was a Christian pastor at the shelter. Guess again. I dialed an ubulanxe to go to the hospital because my teeth were bleeding.and I was coughing up blood. The woman told me I should not stay
…
at Lockport Cares because I called an ambulance to go to the hospital.
I assume Lockport cares is possibly food poisoning people. Lockport cares gives you bag lunches , breakfast and dinner.
For 2 nights there is always corn or brownies during Bible study at 8pm at night.
I'm not allowed back because I claaid they were food poisoning people
I told the police when I dialed the ambulance.
My blood sugar was low and I was coughing up blood and my teeth were bleeding.
Warning. Lockport Cares does food poisoning
Also there is a hazard for COVID 19. The manager allows COVID 19 positive to stay there without mandatory mask
You are not required to wear mask indoors.amd of you are positive for covid 19, you are not required to wear a mask. There is a woman positive for covid 10 not wearing a mask everyday spreading her disease. Lockport Cares allows kids and married couples to stay the night also.
Lockport cares should be shut down for biohazard. Covid positive wear no masks. A mask is not required for covid positive people.
Warning. | Symptoms: Cough
I assume Lockport cares is possibly food poisoning people. Lockport cares gives you bag lunches , breakfast and dinner.
For 2 nights there is always corn or brownies during Bible study at 8pm at night.
I'm not allowed back because I claaid they were food poisoning people
I told the police when I dialed the ambulance.
My blood sugar was low and I was coughing up blood and my teeth were bleeding.
Warning. Lockport Cares does food poisoning
Also there is a hazard for COVID 19. The manager allows COVID 19 positive to stay there without mandatory mask
You are not required to wear mask indoors.amd of you are positive for covid 19, you are not required to wear a mask. There is a woman positive for covid 10 not wearing a mask everyday spreading her disease. Lockport Cares allows kids and married couples to stay the night also.
Lockport cares should be shut down for biohazard. Covid positive wear no masks. A mask is not required for covid positive people.
Warning. | Symptoms: Cough
36
Pet Food, Wyoming, MI, USA
2 weeks ago •reported by user-rqkv1284
Acana cat food made my cats sick almost killing one. MANY brands of pet food are making pets sick and/or killing them. drjudymorgane January 18, 2024 Pet parent consumer reports of bloody diarrhea, vomiting, lethargy, food refusal, feeding: - 4Health - Orijen - Acana - Organix -
…
Blue Buffalo - Pure Balance - Hill's - Purina - Instinct - Royal Canin - Kirkland - Stella & Chewy's - Merrick - Taste of the Wild *This list will be updated as new reports come in 2,012 likes *At this time there are no official recalls for these brands yet. Samples have been sent to an independent laboratory for testing. Toxicology reports pending investigation.
296
R
user-rzfcf411
Hi, you can sign up for email alerts on recalled or food issues at the FDA website. FDA gov
- 1 week ago
- Reply
Power Outage, Wyoming County, NY, USA
8 months ago
Power outages were reported across Western New York as severe thunderstorms rolled across the region. As of 1:00 a.m., National Grid reported more than 8,700 customers who lacked power. The bulk of those customers included more than 4,300 people in Erie County. There were also 3,700 customers
…
lacking power in Chautauqua County, and nearly 750 more in Cattaraugus County on Friday morning. As of 1:00 a.m., NYSEG reported more than 6,200 customers without power, with more than 4,200 of those in Chautauqua County. Over 1,200 people Wyoming County lacked power early Friday morning.
NYSEG: outagemap.nyseg.com/
National Grid: outagemap.ny.nationalgridus.com/
Source: www.wgrz.com/article/weather/severe-weather/power-outages-severe-thunderstorm-rolls-across-wny/71-63535482-baed-46bf-bc8a-82957d299365
Published: 2023-07-20
NYSEG: outagemap.nyseg.com/
National Grid: outagemap.ny.nationalgridus.com/
Source: www.wgrz.com/article/weather/severe-weather/power-outages-severe-thunderstorm-rolls-across-wny/71-63535482-baed-46bf-bc8a-82957d299365
Published: 2023-07-20
3
A SCAM with POSTAGE DUE!, Wyoming, MI, USA
11 months ago •reported by user-rjvp6957
Very small yellow envelope. Return address Says ONLINE SELLER 21005 64th Ave S. Kent WA 98032 There was postage due of $5.15, which I paid the mailman before I was given the envelope. Turns out there was a rip in the envelope and nothing was in it!
…
This is the THIRD TIME this has happened to us. They have all had CHINESE WRITING ON THEM.
296
Power Outage, Wyoming, MI, USA
1 year ago
Thousands of customers lost power Wednesday morning as storms moved through West Michigan. As of around 10:45 a.m. Wednesday, more than 16,428 customers are without power across Michigan, according to the Consumers Energy outage map.
Allegan County: 3,149 customers
Barry County: 426 customers
Ionia County: 185 customers …
Kent County: 3,983customers
Montcalm County: 237 costumers
Ottawa County: 187 customers
Van Buren County: 659 customers
Outage link: www.consumersenergy.com/outagemap
Source: www.woodtv.com/news/michigan/severe-weather-knocks-out-power-to-thousands-across-w-mi/
Published: 2023-04-05
Allegan County: 3,149 customers
Barry County: 426 customers
Ionia County: 185 customers …
Kent County: 3,983customers
Montcalm County: 237 costumers
Ottawa County: 187 customers
Van Buren County: 659 customers
Outage link: www.consumersenergy.com/outagemap
Source: www.woodtv.com/news/michigan/severe-weather-knocks-out-power-to-thousands-across-w-mi/
Published: 2023-04-05
296
Nearly a thousand people are without power Thursday night after a truck crashed into a power pole in Wyoming. The incident happened around 9 p.m. at 44th and Burlingame when a car into a powerline and flipped upside down. Consumers Energy says 850 customers are affected
Outage …
Outage …
76
Recent Interesting Reports
InfuTronix Nimbus Ambulatory Infusion Pump System recalled due to customer complaints, USA
3 weeks ago •source www.fda.gov
Recall notice
InfuTronix, LLC has announced a voluntary recall of the Nimbus Ambulatory Infusion Pump System, including Nimbus II PainPro, Nimbus II Flex, Nimbus II Plus, Nimbus II EpiD and Nimbus II EMS from the US Market due to a high number (3698) of customer complaints related to the
…
Nimbus Infusion Pump systems dated May 2019 to August 2023.
Evaluation of complaint data has identified several potential product issues:
- Battery Power may potentially affect the performance of the pump by causing an immediate power off event.
- Upstream Occlusion, as noted by the upstream occlusion alarm, occurs when there is a block in flow of the proximal end of the administration set.
- System Errors, as noted by the System Error alarm which causes the pump to suspend the infusion.
- Drug product egress from certain administration set bonding points, which may potentially result in drug product leaking from the device.
- Flow Rate (high or low) which may potentially lead to the pump infusing an inaccurate delivery of the drug.
- Pump Housing design which may potentially result in damage over time to certain areas of the housing responsible for administration set engagement, leading to false occlusions and flow rate inaccuracies.
These product issues were identified through the InfuTronix post-market surveillance system and evaluated through the InfuTronix Corrective Action/Preventive Action (CAPA) system. InfuTronix has determined that the best corrective and preventive action to address the identified product issues and potential outcomes is a redesign of the Nimbus Infusion Pump system. The redesign of the system will allow InfuTronix to improve several aspects of the product including mechanics, electronics, software, and housing design as well as aspects of the administration set. Given the number of anticipated design improvements and the extensive requirement for design, verification, and validation, InfuTronix believes a new premarket notification(s) and clearance from FDA may be required. As such, InfuTronix is seeking to remove the system from the market while these improvements and design changes are being made and a new clearance(s) is obtained.
A health hazard evaluation (HHE) was performed by an independent physician to evaluate routine post-market complaint failure modes associated with the Nimbus family of infusion pumps. The HHE determined that the common device failure modes pose a low risk to users.
The Nimbus Infusion Pump system has been distributed throughout the United States since October 17, 2014 until February 21, 2024. It has never been distributed internationally. Affected devices have the following Unique Device Identification numbers associated with them:
- Nimbus Ambulatory Infusion Pump 00817170020000
- Nimbus II PainPRO 00817170020086
- Nimbus II Flex 00817170020093
- Nimbus II Plus 00817170020161
- Nimbus II EpiD 00817170020376
- Nimbus II EMS 00817170020109
Users may continue to use the Nimbus Infusion Pump system and associated infusion sets during this removal process. Users should be aware of the signs indicating a potential issue with the pump (How to recognize that a device may fail):
- Battery – The infusion pump will brown out (fail-safe). The user will see that the pump has shut off. Additionally, the LED screen may flicker prior to failure, indicating a potential battery issue.
- Upstream Occlusion - Auditory and visual occlusion alarm alerts the user of the occlusion.
- System Error - Auditory and visual system error alarm will alert the user.
- Drug Product Egress – The user may notice leaking drug from the pump pouch or infusion set or feel wetness from the drug product.
- Flow Rate (high/low) - Auditory and visual occlusion alarm for low flow will alert the user of occlusion. The user will notice residual volume remaining at the end of therapy. High flow rate may be associated with shortened infusion times.
- Pump Housing Damage - The user may notice broken latches, hinges, or cracks in the housing and/or user may notice that the device is difficult to assemble prior to use.
Infutronix has already notified customers with a letter that details the products impacted, reason for the voluntary removal, risk to health assessment, how to recognize the device may fail and actions to be taken by the customer/user.
The continued use of the Nimbus Infusion Pump system and associated infusion sets is safe during this removal process. Users should be aware of the signs indicating a potential issue with the pump as described above, “How to recognize that a device may fail”. As with any use, health care providers (HCPs) should read the Instructions for Use (IFU) and follow those closely to ensure proper performance of the pump with its associated accessory set. Further, HCPs should educate patients on proper use of the pump and accessories, and potential operational concerns. As a reminder to HCPs,
- When replacing batteries, only new batteries should be used. Care should be taken to ensure that old and new batteries are not confused when completing the replacement. When resetting the battery state, HCPs are encouraged to pay close attention to the device indicator lights and LED screen indicating battery life.
- HCPs should take care to clear an occlusion alarm properly. The battery should not be cycled (turned on/off) to clear the occlusion alarm. If the occlusion alarm cannot be cleared, a new pump should be used. Patients should be educated that silencing the alarm does not clear the occlusion.
- Due to the potential ambulatory use of the pump, patients may carry the drug product dispensing pouch in a carrying pack. Patients should be educated that impeding the tubing set or placing pressure on the device (leaning against it, sitting on it) may cause the device to malfunction.
- HCPs are encouraged to educate patients on potential drug leakage and establish appropriate containment protocols for users to follow.
HCPs should ensure users are educated to recognize audio and visual alarms and inspect their device for damage. Any difficulties or abnormalities noted with the pump or accessories should result in immediate discontinued use of the pump and notification to the HCP. Customers of InfuTronix who have Nimbus Infusion Pumps and associated infusion sets in their possession should contact InfuTronix customer service, where they will be instructed on the Return Material Authorization (RMA) process to be followed for returning both the Nimbus Infusion Pumps and associated infusion sets.
Customers who purchase the Nimbus Infusion Pump and/or associated infusion sets from a distributor should contact their distributor directly and receive instructions on the RMA process to be followed. As the device will not be available or supported after June 20, 2024, InfuTronix encourages the healthcare provider to seek alternative methods of drug product infusion appropriate for their patient’s needs, based on their medical expertise, at the earliest possible opportunity. InfuTronix is removing the Nimbus Infusion Pump Systems from the market.
The products will no longer be supported by InfuTronix for either Nimbus Infusion Pumps or related infusion sets beyond June 20, 2024. To return Nimbus products customers should follow the instructions provided in the Medical Device Removal letter that was sent by InfuTronix, contact InfuTronix customer service or their local distributor.
Company name: InfuTronix, LLC
Brand name: Nimbus
Product recalled: Nimbus Pump System
Reason of the recall: Recall due to a high number (3698) of customer complaints related to the Nimbus Infusion Pump systems
FDA Recall date: March 20, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-removal-announcement-infutronix-nimbus-ambulatory-infusion-pump-system
Evaluation of complaint data has identified several potential product issues:
- Battery Power may potentially affect the performance of the pump by causing an immediate power off event.
- Upstream Occlusion, as noted by the upstream occlusion alarm, occurs when there is a block in flow of the proximal end of the administration set.
- System Errors, as noted by the System Error alarm which causes the pump to suspend the infusion.
- Drug product egress from certain administration set bonding points, which may potentially result in drug product leaking from the device.
- Flow Rate (high or low) which may potentially lead to the pump infusing an inaccurate delivery of the drug.
- Pump Housing design which may potentially result in damage over time to certain areas of the housing responsible for administration set engagement, leading to false occlusions and flow rate inaccuracies.
These product issues were identified through the InfuTronix post-market surveillance system and evaluated through the InfuTronix Corrective Action/Preventive Action (CAPA) system. InfuTronix has determined that the best corrective and preventive action to address the identified product issues and potential outcomes is a redesign of the Nimbus Infusion Pump system. The redesign of the system will allow InfuTronix to improve several aspects of the product including mechanics, electronics, software, and housing design as well as aspects of the administration set. Given the number of anticipated design improvements and the extensive requirement for design, verification, and validation, InfuTronix believes a new premarket notification(s) and clearance from FDA may be required. As such, InfuTronix is seeking to remove the system from the market while these improvements and design changes are being made and a new clearance(s) is obtained.
A health hazard evaluation (HHE) was performed by an independent physician to evaluate routine post-market complaint failure modes associated with the Nimbus family of infusion pumps. The HHE determined that the common device failure modes pose a low risk to users.
The Nimbus Infusion Pump system has been distributed throughout the United States since October 17, 2014 until February 21, 2024. It has never been distributed internationally. Affected devices have the following Unique Device Identification numbers associated with them:
- Nimbus Ambulatory Infusion Pump 00817170020000
- Nimbus II PainPRO 00817170020086
- Nimbus II Flex 00817170020093
- Nimbus II Plus 00817170020161
- Nimbus II EpiD 00817170020376
- Nimbus II EMS 00817170020109
Users may continue to use the Nimbus Infusion Pump system and associated infusion sets during this removal process. Users should be aware of the signs indicating a potential issue with the pump (How to recognize that a device may fail):
- Battery – The infusion pump will brown out (fail-safe). The user will see that the pump has shut off. Additionally, the LED screen may flicker prior to failure, indicating a potential battery issue.
- Upstream Occlusion - Auditory and visual occlusion alarm alerts the user of the occlusion.
- System Error - Auditory and visual system error alarm will alert the user.
- Drug Product Egress – The user may notice leaking drug from the pump pouch or infusion set or feel wetness from the drug product.
- Flow Rate (high/low) - Auditory and visual occlusion alarm for low flow will alert the user of occlusion. The user will notice residual volume remaining at the end of therapy. High flow rate may be associated with shortened infusion times.
- Pump Housing Damage - The user may notice broken latches, hinges, or cracks in the housing and/or user may notice that the device is difficult to assemble prior to use.
Infutronix has already notified customers with a letter that details the products impacted, reason for the voluntary removal, risk to health assessment, how to recognize the device may fail and actions to be taken by the customer/user.
The continued use of the Nimbus Infusion Pump system and associated infusion sets is safe during this removal process. Users should be aware of the signs indicating a potential issue with the pump as described above, “How to recognize that a device may fail”. As with any use, health care providers (HCPs) should read the Instructions for Use (IFU) and follow those closely to ensure proper performance of the pump with its associated accessory set. Further, HCPs should educate patients on proper use of the pump and accessories, and potential operational concerns. As a reminder to HCPs,
- When replacing batteries, only new batteries should be used. Care should be taken to ensure that old and new batteries are not confused when completing the replacement. When resetting the battery state, HCPs are encouraged to pay close attention to the device indicator lights and LED screen indicating battery life.
- HCPs should take care to clear an occlusion alarm properly. The battery should not be cycled (turned on/off) to clear the occlusion alarm. If the occlusion alarm cannot be cleared, a new pump should be used. Patients should be educated that silencing the alarm does not clear the occlusion.
- Due to the potential ambulatory use of the pump, patients may carry the drug product dispensing pouch in a carrying pack. Patients should be educated that impeding the tubing set or placing pressure on the device (leaning against it, sitting on it) may cause the device to malfunction.
- HCPs are encouraged to educate patients on potential drug leakage and establish appropriate containment protocols for users to follow.
HCPs should ensure users are educated to recognize audio and visual alarms and inspect their device for damage. Any difficulties or abnormalities noted with the pump or accessories should result in immediate discontinued use of the pump and notification to the HCP. Customers of InfuTronix who have Nimbus Infusion Pumps and associated infusion sets in their possession should contact InfuTronix customer service, where they will be instructed on the Return Material Authorization (RMA) process to be followed for returning both the Nimbus Infusion Pumps and associated infusion sets.
Customers who purchase the Nimbus Infusion Pump and/or associated infusion sets from a distributor should contact their distributor directly and receive instructions on the RMA process to be followed. As the device will not be available or supported after June 20, 2024, InfuTronix encourages the healthcare provider to seek alternative methods of drug product infusion appropriate for their patient’s needs, based on their medical expertise, at the earliest possible opportunity. InfuTronix is removing the Nimbus Infusion Pump Systems from the market.
The products will no longer be supported by InfuTronix for either Nimbus Infusion Pumps or related infusion sets beyond June 20, 2024. To return Nimbus products customers should follow the instructions provided in the Medical Device Removal letter that was sent by InfuTronix, contact InfuTronix customer service or their local distributor.
Company name: InfuTronix, LLC
Brand name: Nimbus
Product recalled: Nimbus Pump System
Reason of the recall: Recall due to a high number (3698) of customer complaints related to the Nimbus Infusion Pump systems
FDA Recall date: March 20, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-removal-announcement-infutronix-nimbus-ambulatory-infusion-pump-system
303
Fake product, not what I ordered, Libby, MT, USA
3 weeks ago •reported by user-rwtmr233
Thought a injured veteran made a product. What I received is a fake paper product. Can I get. Refund ?
4
Heathers Mottsy, Staten Island, NY, USA
1 week ago •reported by user-bgktg429
SKAM!!!!!!!!! I ordered a cross made out of horseshoes. Pieces were plastic and very small. Not cut right so nothing fit together. Worthless piece of junk! Had to try to put it together with many pieces and it is crooked and warped looking.
SCAM!!!!!!!!!!!!!!
SCAM!!!!!!!!!!!!!!
163
Unauthorized Credit Card Charge from Peggy Piercy, Virginia Beach, VA, USA
1 week ago •reported by user-cfjm3464
I received a package containing SUBGENIX BIORIBOSE. MY OLD CARD WAS BILLED FOR THIS I didn't order it. Subsequently my card was cancelled. I'm waiting for my new one. I'm 20lbs under weight, the last thing I need is a weight loss supplement.
582
Didn't get what I paid for, Princeton, IL, USA
3 weeks ago •reported by user-vjcyr133
I was supposed to receive a pallet of goods and I got 1 pair of wireless earbuds
5
I did not order this product, Greenbelt, Maryland, USA
3 days ago •reported by user-hnby3436
I did not order this KETO PURE
278
Unordered Package, 2800 N Franklin Rd, Indianapolis, IN 46219, USA
2 days ago •reported by user-xcwhw738
I received a package from "ROSEWOOD P," 2800 N Franklin Rd. Indianapolis IN, 46219. I did not order anything from this person or address nor have I ever ordered from them. Please check this out. I'm in Visalia, CA USA. Thank you
Item is a metal cylinder …
Item is a metal cylinder …
about 1" in length and the top third of it has a hard plastic sleeve covering it. There was no receipt, order form or shipping information inside the bubble pack shipped via UPS Ground Advantage, USPS Tracking # 934 6361 1032 2950 244****.
347
Scam - ketogenesis. com, Las Vegas, NV, USA
1 week ago •reported by user-kybcp695
I want to cancel my order & there is no number to call. I want a refund!!!
1.4K
Safety issue, I got this in the mail two little tags
3 weeks ago •reported by user-jqqk9321
I can send a pic of the package and what was in it
I recieved a ring i never ordered, Yucca Ave, Lancaster, L A, CA, USA
1 week ago •reported by user-grgz1638
a white envelope came theough ups from yoshi deals tracking #9200111109483252937419**** the object was in a red ring box
107
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