Burger King, 4200 International Boulevard, OAKLAND, CA, 94601, USA
Latest report:
Covid-19 OSHA Complaint
3 years ago
1. The employer is failing to send home employees who report feeling ill or showing signs and symptoms of COVID-19. Employees in November and December reported feeling ill and were asked to take medicine and stay at work. T8 CCR 3205(c)(4) 2. The employer is failing to
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notify and/or quarantine close contacts to employees who were suspected of having COVID-19. Employees in November and December all spent time at home away from work and no employees were notified or quarantined for close contact exposure. T8 CCR 3205(c)(3)(b)(3)(a) 3. The employer is failing to screen employees for signs and symptoms when they come to work. Management does not ask questions if employees are having signs or symptoms. T8 CCR 3205(c)(2)(B) 4. The employer is failing to train employees in the topics of COVID-19, such as social distancing and cleaning of high touch areas. T8 CCR 3205(c)(5) 5. The employer is failing to ensure that all practical solutions are in place to maintain social distancing. The chicken and fry station are in close proximity and sometimes is close to the drive thru station. Management has not adjusted the work schedule to allow for more social distancing. T8 CCR 3205(c)(6)(A) 6. The employer failed to implement a written plan for COVID-19 with policy and procedures. There is not a written plan in place to outline how often areas are cleaned, how often employees are to wash their hands, and how to maintain as much social distancing as possible. T8 CCR 3205(c) 7. The employer is failing to enforce that employees wash their hands frequently while in the workplace. T8 CCR 3205(c)(8)(D) 8. The employer is failing to ensure that high touch areas are cleaned frequently. T8 CCR 3205(c)(8)(C)
Alleged Hazards: 8, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-26
Alleged Hazards: 8, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-26
221
Recent Interesting Reports
Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA
2 weeks ago •source www.fda.gov
Recall notice
Honeywell Safety Products USA, Inc. is voluntarily recalling Fendall 2000 Non-Sterile Eyewash Cartridge for the Fendall 2000 Eyewash Station. This recall is being conducted at the industrial consumer level. Honeywell’s supplier of the Fendall 2000 Non-Sterile Eyewash Cartridge has been found to be non-compliant with current good
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manufacturing practice (cGMP) requirements. To date, Honeywell Safety Products USA, Inc. has not received any reports of adverse events related to this recall.
The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651
Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.
Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.
Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024
Source: www.fda.gov
The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651
Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.
Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.
Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024
Source: www.fda.gov
303
Receipt of an item I didn't order, Beech Grove, IN, USA
3 weeks ago •reported by user-pmgck436
I received an item in the mail, a men's wrist watch, I did not order in the mail today. It was sent to my mail and address but I did not order anything like this from anywhere. The Sender's name and address are Cindy Zhang, 585 Johnson Avenue #3DBOHEMIA, Bohemia, NY 11716.
127
Scam, Saskatchewan, Canada
1 day ago •reported by user-jczyy898
I submitted a report about a hydrogen bottle that did not have an outlet for a plug in.
I ordered a hydrogen bottle from YW Co. Ltd, from Mississauga, ON. and there is no outlet on the bottom of the bottle for any plug in. I emailed …
I ordered a hydrogen bottle from YW Co. Ltd, from Mississauga, ON. and there is no outlet on the bottom of the bottle for any plug in. I emailed …
about the problem and they sent another plug in for the unit, but there no outlet for a plug in. I want a refund.
9
Heathers Mottysy, 1655 Richmond Ave, Staten Island, NY, USA
2 weeks ago •reported by user-xgxp2235
Bought a wood carving of a male & female about to kiss , was supposed to have a nice stained finish. Product I received was raw wood unfinished and very cheaply made!!
Big scam !!!
Big scam !!!
2.9K
I keep receiving more when I canceled this in January, Bethlehem, PA, USA
1 week ago •reported by user-ykxqg698
Just received an order for $190 and would like to return it for a refund
184
I received a package I did not order!, Greenwood, IN, USA
2 days ago •reported by user-pzqzx691
I am receiving unordered keto crap from Fullfillmen Housr in Tampa! Fullfillment house
127
I didn't order a smart watch, Walton Street, Durham, NC, USA
2 weeks ago •reported by user-xjtyj214
I didn't receive the package I ordered. I didn't order a smart watch this is a fake.. everyone be aware
This company is a fake I didn't receive the box that was advertised
This company is a fake I didn't receive the box that was advertised
275
I ordered an induction product and something came that I don't need
toate reclemele care ajung pe facebook cu produse din china o sa le raportez
toate reclemele care ajung pe facebook cu produse din china o sa le raportez
I can not find a number to cancel my subscription that i did not agree too, South Carolina, USA
6 days ago •reported by user-kmdn3584
I ordered a one time for 199.00 and they keep billing and sending gummies
115
I received a bottle of Keto Pure Bioribose I didn't request. I don't know how or why I received it., Somers, WI, USA
8 hours ago •reported by user-ykkyz882
Return address: Fulfillment House, PO BOX 5708, Tampa FL 33675-5708. Received on Apr 18, 2024. Don't know why or how!
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