Kaiser Permanente Oakland Medical Center, 3600 Broadway, OAKLAND, CA, 94611, USA
Latest report:
Report by
Covid-19 OSHA Complaint
2 years ago
Oxygen has been leaking continuously in patient room #1061 on the 10th South Unit and has been allowed to accumulate in the room instead of being repaired. T8 CCR 5507(c)
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-11-29
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-11-29
380
Covid-19 OSHA Complaint
2 years ago
The employer failed to ensure that the HVAC system is maintained and operated as required by Title 24, Part 2. Indoor temperatures have exceeded 80 degrees Fahrenheit, and ventilation had been limited or stopped entirely. T8 CCR 5142(a) and 3205(c)(7)(A)
Alleged Hazards: 1, Employees Exposed: 5
Source:
Alleged Hazards: 1, Employees Exposed: 5
Source:
Osha.gov | Receipt Date: 2021-10-29
380
Covid-19 OSHA Complaint
3 years ago
1. The employer failed to use airborne isolation infection precautions for a suspected COVID-19 case by downgrading the airborne precautions for a novel virus as described in Appendix A to droplet precautions. T8 CCR 5199 2. The employer failed to provide necessary personal protection equipment to employees
who may provide care to suspected COVID-19 cases as prescribed for novel viruses in Appendix A and section 5199(g). T8 CCR 5199 3. The employer failed to ensure that respirators are stored to protect them from contamination. Contaminated respirators are stored in bags or pockets and later reused. T8 CCR 5199
Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-18
Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-18
380
Covid-19 OSHA Complaint
3 years ago
1. The employer failed to use airborne isolation infection precautions for a suspected COVID-19 case by downgrading the airborne precautions for a novel virus as described in Appendix A to droplet precautions. T8 CCR 5199 2. The employer failed to provide necessary personal protective equipment to employees
who may provide care to suspected COVID-19 cases as prescribed for novel viruses in Appendix A and section 5199(g). T8 CCR 5199 3. The employer failed to ensure that respirators are stored to protect them from contamination. Contaminated respirators are stored in bags or pockets and later reused. Contaminated face shields are shared and reused. T8 CCR 5199 4. The employer failed to provide a powered air purifying respirator (PAPR) with a High Efficiency Particulate Air (HEPA) filter(s), or a respirator providing equivalent or greater protection, to employees who perform high hazard procedures on COVID-19 cases or suspected cases. T8 CCR 5199 5. The employer failed to establish and maintain internal safety guidelines requiring Hand Hygiene Observers during the doffing of contaminated personal protective equipment. T8 CCR 5199
Alleged Hazards: 5, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-18
Alleged Hazards: 5, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-18
380
Covid-19 OSHA Complaint
3 years ago
1. The employer is failing to use airborne isolation infection precautions for a suspected COVID-19 case by downgrading the airborne precautions for a novel virus described in Appendix A to droplet precautions in the Labor/Delivery Department. T8 CCR 5199(e)(1)(A) 2. The employer failed to provide the necessary
personal protective equipment to employees who are providing care to isolated patients diagnosed with COVID-19. The manager is keeping all N95 respirators, bleach and sanitizing wipes locked away in their office where employees cannot access them. T8 CCR 5199(e)(1) 3. The employer is failing to correct hazards of having employees use only one mask the whole shift while not being able to reuse masks and faces shields when exposed to COVID-19 patients and potentially exposing over patients and themselves. T8 CCR 5199(e)(2)
Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-23
Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-23
380
Covid-19 OSHA Complaint
3 years ago
1. The employer failed to provide the necessary personal protective equipment to employees who are providing care to patients diagnosed with COVID-19 and rule out patients throughout the hospital. T8 CCR 5199(e)(1) 2. The employer is failing to correct hazards of having employees use only one mask
the whole shift while not being able to reuse masks and face shields when exposed to COVID-19 patients and potentially exposing over patients and themselves. T8 CCR 5199(e)(2)
Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-23
Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-23
380
Covid-19 OSHA Complaint
3 years ago
The employer failed to provide necessary personal protective equipment to the phlebotomy team who may be exposed to COVID-19. Employees are not provided with gloves, and employees collecting samples or performing procedures capable of aerosolizing COVID-19 are not provided with respiratory protection as prescribed for novel viruses
in Appendix A and section 5199(g). T8 CCR 5199(f)
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-18
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-03-18
380
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Tejocote Dietary Supplements - recalled because it contains toxic yellow oleander, USA
3 weeks ago •source www.fda.gov
Recall notice
Global Mix, Inc. of New York, is recalling tejocote products to include the following brands: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra. The recalled products are labeled as tejocote root but are toxic yellow oleander. The recalled products were distributed in the following states: AL, AK,
CA, CO, CT, DE, FL, GA, HI, ID, IL, IA, IN, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NM, NC, NY, NJ, ND, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV, WI, and WY through website. The recalled products were also sold via the below websites via courier direct delivery and mail order. Etsy, amazon, eva-nutrition, tejocotemexican, niwali, scienceofalpha. The recalling firm has not received any reported of illness.
Recalled Products include the following bearing below information. Product codes and expiration dates can be found on the bottom of the packaging.
Product Name: Eva Nutrition MexicanTejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Science of Alpha Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: NWL Nutra Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Niwali Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Per the safety alert update on 3/12/24, "The FDA continues to receive adverse event reports related to the products identified in this Safety Alert."
The recall was the result of a routine sampling program by the company which revealed that the finished products contained the yellow oleander. The company has ceased the production and distribution of the product as the company continues their investigation as to what caused the problem. Further the company is conducting comprehensive quality control and monitoring process.
Customers who have purchased these products should stop using them immediately and return them to the point of purchase for a full refund.
Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.
If you are experiencing symptoms after eating this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Company name: Global Mix, Inc.
Brand name: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra
Product recalled: Tejocote Dietary Supplements
Reason of the recall: Product contains toxic yellow oleander.
FDA Recall date: April 10, 2024
Source: www.fda.gov
Recalled Products include the following bearing below information. Product codes and expiration dates can be found on the bottom of the packaging.
Product Name: Eva Nutrition MexicanTejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Science of Alpha Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: NWL Nutra Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Niwali Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Per the safety alert update on 3/12/24, "The FDA continues to receive adverse event reports related to the products identified in this Safety Alert."
The recall was the result of a routine sampling program by the company which revealed that the finished products contained the yellow oleander. The company has ceased the production and distribution of the product as the company continues their investigation as to what caused the problem. Further the company is conducting comprehensive quality control and monitoring process.
Customers who have purchased these products should stop using them immediately and return them to the point of purchase for a full refund.
Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.
If you are experiencing symptoms after eating this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.
Company name: Global Mix, Inc.
Brand name: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra
Product recalled: Tejocote Dietary Supplements
Reason of the recall: Product contains toxic yellow oleander.
FDA Recall date: April 10, 2024
Source: www.fda.gov
303
I received a package in the mail today that i never heard of nor ordered., Eastpointe, MI, USA
3 weeks ago •reported by user-wjzp6244
I received this package in the mail and I never ordered anything, from this place called Fullfillment House PO Box 10205 Tampa FL 33679-0205, they have charged me 3 x on my credit card, first charges was on March 24 2024 one charge for $ 60.09, and
another charge for $99.00 on the same day, then again on April 4 2024 for 60.09.
111
Last 30 days