Burger King, 7201 Fair Oaks Blvd, Carmichael, CA 95608, USA
Latest report:
Covid-19 OSHA Complaint
3 years ago
3203(a)(4): Employees are not required to wear facial covering and not maintaining social distancing. On September 18, 2020, partial inspection of the site was conducted. The employer was operating a fast food restaurant, and there were approximately four employees observed during the course of the inspection. The
…
employer¿s written programs were reviewed and were found to be in compliance with T8CCR requirements and COVID-19 Guidelines.
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-06
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-06
577
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Burger King, Gaußstrasse, Dachau, Germany, Burger King, Gaußstraße, Dachau, Deutschland
6 months ago •reported by user-hmqn9499
If impudence is written with a capital letter, it's there!
I was at this restaurant with a friend around 12:05pm. Behind the counter was a new employee and her supervisor (wearing a white blouse).
We asked a question about the order and were completely ignored! When the …
I was at this restaurant with a friend around 12:05pm. Behind the counter was a new employee and her supervisor (wearing a white blouse).
We asked a question about the order and were completely ignored! When the …
lady in the white blouse wanted to dedicate herself to us, I told her that we had actually already asked a question and received no answer.
The “very nice lady” with the white blouse then said she couldn't cut into quarters and we should do our “Sch...” ourselves, she would leave now. The employee to be trained was visibly shocked by this attitude.
I told her she'd better keep her burgers and I'd go somewhere else. The very nice lady then said that we should leave the restaurant and never come back! She could do without us!
So this restaurant, which really also has questionable reviews on other portals, really never sees us again!
The customer here is just a troublemaker and not welcome. Quite apart from outrageous insults...
The “very nice lady” with the white blouse then said she couldn't cut into quarters and we should do our “Sch...” ourselves, she would leave now. The employee to be trained was visibly shocked by this attitude.
I told her she'd better keep her burgers and I'd go somewhere else. The very nice lady then said that we should leave the restaurant and never come back! She could do without us!
So this restaurant, which really also has questionable reviews on other portals, really never sees us again!
The customer here is just a troublemaker and not welcome. Quite apart from outrageous insults...
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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.
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Safety violation in Burger King store, Burger King, Spine Road, Boulder, Colorado 80301, USA
8 months ago •reported by user-qzqd1881
My husband sustained a skin tear when we were at the store. A piece of metal was sticking out the counter and as he was lifting his foot, the metal piece cut his foot. Obviously he did not see the metal piece that was sticking out. The
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store manager refused to help us, stated "Its not my problem" and never apologized. He never went to see what the problem was or even took care of the metal piece that still is sticking out the counter. He refused to give us his name and ignored us completely. This is the worst customer service !!! the manager completly ignors a safety concern and hides behind the counter and acts like we are causing trouble? so if someone really gets hurt at this store, no one is accountable? that's a good case for a law suit! This is the worst store ever and people like that should not even work there! this manager has the worst customer service skills and has not concept of safety and very ill-manered person who clearly hates his job and doesn't care about customers or even his employees! Fix the damn problem greedy business corporates!
115
They don't take good care of you, Burger King ® Copec San Martin - Caletera Ote. Gral. San Martín, Quilicura, Colina, Región Metropolitana, Chile
8 months ago •reported by user-jkmmt979
I went shopping at the place that is on the San Martin road, hill I received my order in the van and the children's box that pays for didn't come, besides, canceling extra juice and compote, the attention is too fast that they throw your orders in
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the car, and they ask you to move forward that you don't have time to check, and on both occasions when you pay and receive your food they don't serve you well.
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Outage link: myaccount.smud.org/manage/outage
Source: fox40.com/news/local-news/sacramento-county/more-than-3000-smud-customers-without-power/
Published: 2023-12-18
Outage link: myaccount.smud.org/manage/outage
Source: fox40.com/news/local-news/sacramento-county/more-than-3000-smud-customers-without-power/
Published: 2023-12-18
577
Package I didn’t order, Carmichael, CA, USA
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I received a pair of sunglasses I didn’t order.
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10 months ago
Nearly 20,000 people were without power Saturday evening due to an unplanned outage, according to SMUD
Outage link: www.smud.org/en/Customer-Support/Outage-Status
Source: www.abc10.com/article/news/local/power-outage-carmichael-smud/103-b72bfc7b-e401-4907-ba3d-8daa19b1fc45
Published: 2023-05-27
Outage link: www.smud.org/en/Customer-Support/Outage-Status
Source: www.abc10.com/article/news/local/power-outage-carmichael-smud/103-b72bfc7b-e401-4907-ba3d-8daa19b1fc45
Published: 2023-05-27
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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
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.
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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
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