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A
1. The employer failed to develop and implement a process for screening employees for and responding to employees with COVID-19 symptoms. The employer only screens occasionally, but not on a daily basis. Title 8 CCR §3205(c)(2)(B) 2. The employer failed to provide face coverings. The employer tells … See More
employees that if they don't have a facemask, they should go home' Title 8 CCR §3205(c)(6)(B) 3. The employer failed to review applicable orders and guidance from the State of California and the local health department related to COVID-19 hazards and prevention. Several employees are not following the most recent Alameda County orders that require all people, regardless of vaccination status, to wear face coverings indoors. The employees on the late shift will constantly wear their facemasks below their nose. Title 8 CCR §3205(c)(2)(F) 4. The employer failed to give written notice, within one business day, that people at the worksite may have been exposed to COVID-19. Written notice may include, but is not limited to, personal service, email, or text message if it can reasonably be anticipated to be received by the employee within one business day of sending. The notice shall include the disinfection plan required by Labor Code section 6409.6(a)(4). There have been at least 2 COVID-19 cases present in the workplace and all employees were not notified. The employer didn't notify any close contacts of cases that resulted in mid March 2021 and late March/Early April of 2021. Title 8 CCR §3205(c)(3)(B)(3) 5. The employer failed to provide effective training and instruction to employees that includes the following: information regarding COVID-19-related benefits to which the employee may be entitled under applicable federal, state, or local laws. This includes any benefits available under legally mandated sick and vaccination leave, if applicable, workers' compensation law, local governmental requirements, the employer's own leave policies, leave guaranteed by contract, and this section. As well as training in the importance of frequent hand washing with soap and water for at least 20 seconds and using hand sanitizer when employees do not have immediate access to a sink or hand washing facility. Additionally, training in public health measures to prevent the spread of COVID-19. The employees don't have an understanding when they should get paid for time off due to covid related items as their paystubs don't show when that time was different from regular time. Title 8 CCR §3205(c)(5)(B) & (C) & (D) & (F) 6. The employer failed to implement cleaning and disinfecting procedures, which require Identifying and regularly cleaning frequently touched surfaces and objects and cleaning of areas, material, and equipment used by a COVID-19 case during the high-risk exposure period, and disinfection if the area, material, or equipment is indoors and will be used by another employee within 24 hours of the COVID-19 case. These cleanings are not being done as needed' Title 8 CCR §3205(c)(7)(B) 7. The employer failed to exclude COVID-19 cases and employees who had a close contact with COVID-19 cases. This occurred in mid March 2021 and late March/early April 2021 as employees felt their were close contacts.. Title 8CCR §3205(c)(9)(A) & (B)

Alleged Hazards: 6, Employees Exposed: 3
Source: Osha.gov | Receipt Date: 2021-09-14
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#coronaviruscovid19 #osha #jackinthebox #3035castrovalleyboulevard #castrovalley #california #us

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Heather's Motty, 2207 Summit Avenue, Union City, NJ, USA

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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 … See More
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
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