Crownview Co-Occurring Institute Incorporated, 315 North Clementine Street, OCEANSIDE, CA, 92054, USA
Latest report:
Covid-19 OSHA Complaint
2 years ago
T8 CCR 5199(c)(5) PPE is not being provided to employees in adequate amounts. There is a lack of masks at several of locations, N-95s are not being provided to employees in direct contact with clients who have tested positive at the facility. T8 CCR 5199(c)(2) Employees are
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ill and report symptoms to employer but are asked to come to work without proper precautions . Some of these employees have since tested positive for COVID-19. The employer is not implementing social distancing at the work place and held a secret santa lunch where social distancing was not practiced. T8 CCR 5199(c) Employer is not conducting exposure investigations to determine employee contact with positive cases during the course of their work and is not properly notifying employees of their potential exposure. Employer is not covering costs of COVID-196 testing for employees who have been exposed at work. T8 CCR 5199(c)(6)(B) Employer is not receiving recommendations from physicians as to whether or not employees should be subject to precautionary removal from workplace due to exposure.
Source: Osha.gov | Receipt Date: 2021-01-04
Source: Osha.gov | Receipt Date: 2021-01-04
425
Covid-19 OSHA Complaint
3 years ago
T8 CCR 5199(c)(3) Employees share face shields and are not provided with adequate PPE. Trash bags are used as gowns. T8 CCR 5144(f) No fit testing for N95. T8 CCR 5144 (e) No medical evaluation. T8 CCR 5199(c)(6)(B) No exposure incidents.
Alleged Hazards: 3, Employees Exposed: 1 …
Source: Osha.gov | Receipt Date: 2020-12-29
Alleged Hazards: 3, Employees Exposed: 1 …
Source: Osha.gov | Receipt Date: 2020-12-29
425
Recent Interesting Reports
Receiving a package that I did not order, 1657 Chaparral trail, Sanford, MI 48657, USA
3 weeks ago •reported by user-dbjqn471
I received some sort of electronic item. Not a clue what it is nor what it’s for .
The return address is:
21460 Yellow brick rd
Walnut , Ca 91789
The return address is:
21460 Yellow brick rd
Walnut , Ca 91789
42
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
I can not find a number to cancel my subscription that i did not agree too, South Carolina, USA
1 week ago •reported by user-kmdn3584
I ordered a one time for 199.00 and they keep billing and sending gummies
115
Unordered Subsonic bioribose, California, USA
3 weeks ago •reported by user-pvtc8992
Grey plastic envelope.Sent via UPS Ground Advantage. Sender : Fulfillment House POBox 10205
Tampa
Flir8da 33679-3147
Tampa
Flir8da 33679-3147
288
disc not working, Hanson, MA, USA
4 weeks ago •reported by user-fqxth686
I received two disc for free cable but it has nothing in them. how to get a refund
86
Received daily detox did not order, Jamestown, TN, USA
1 week ago •reported by user-qwdky314
Received a bottle of daily detox and keto gummies did not order
1
Received 4 camera's that don't work. Unable to find any method to contact EIE CORP., Courtenay, BC, Canada
1 week ago •reported by user-bjnd4693
Camera's shown on TV. 3 easy steps. After 3 knowledgeable people tried to enter data, with no results, I paid a Computer Tech to install these 3 easy steps. He was finally able to enter the data but he said it was not easy. None of the
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cameras would hold a charge after numerous attempts. Any attempt to contact EIE CORP was unsuccessful. Address: EIE CORP UNIT 13-1030 KANATO RD MISSISSAUGA ON L4W 4B6 TRACKING NUMBER 2012 5595 92** **** ORDER NO. YT2405921266****** VIN/NIF 448 SPEC 3696 V2 SKU
Estimated delivery 13 March 2024 Sender EAGLE INTERNATIONAL From L4W4B6 To COURTENAY, BC Origin China Destination Canada Weight 0.297 kg Next tracking numbers
Estimated delivery 13 March 2024 Sender EAGLE INTERNATIONAL From L4W4B6 To COURTENAY, BC Origin China Destination Canada Weight 0.297 kg Next tracking numbers
15
Received strange poorly wrapped package, Chagrin Falls, OH, USA
4 weeks ago •reported by user-kqzmv138
Never ordered anything from the alleged seller/scammer. Package is cake box size and weighty. Did not open it. Could be anything in there, including harmful stuff. Checking cards to see if someone illegally charged me. Reporting this as a fraud and scam by the alleged unnamed "online
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seller" at 3646 S. Wolcott Ave., Chicago, Il, 60609. I demand law enforcement do a P Diddy type raid on this place and bring these scammers down now!!
Very suspect.
Very suspect.
98
Dream Bones Sick, Mexico City, CDMX, Mexico
1 week ago •reported by user-hyhtp455
My 5-year-old champion vomited and is very depressed after eating the “dreambone” awards,
| Symptoms: Vomiting
55
received an unsolicited package of Subgenix-bioribose, Warwick, RI, USA
2 weeks ago •reported by user-kpvbj826
received a package of Subgenix bioribose that i did not order. i am monitoring all of my accounts to make sure whomever sent this unsolicited package does not take my money!
271
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