West Hills Hospital and Medical Center, 7300 Medical Center Dr., WEST HILLS, CA, 91307, USA
Latest report:
Covid-19 OSHA Complaint
2 years ago
Employer failed to adhere to health and safety regulations mandating protective measures and plans. ER failed to maintain and supply adequate PPE. Employer failed to provide adequate staff and staffing rations creating unsafe working conditions and inability to monitor and ensure other staff donning and doffing of
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PPE. ER failed to comply with or adequately follow mandated Aerosol Transmissible Diseases Exposure Control Plan (ATD) standards. ER unreasonably exposing employees and staff to COVID without adequate safety protocols and PPE. Employer mandated unsafe conduct and procedures related to PPE and denial of use of equipment intended to protect employees from Covid.
Source: Osha.gov | Receipt Date: 2020-12-04
Source: Osha.gov | Receipt Date: 2020-12-04
468
Covid-19 OSHA Complaint
2 years ago
California Code of Regulations, Title 8, Section 5120(c)(5)(C). Health Care Worker Back and Musculoskeletal Injury Prevention. There is no lift equipment or other trained staff available to assist a nurses in pulling up patients in bed, or transferring patients to another bed or chair. California Code of
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Regulations. Title 8, Section 5199(e)(l), Aerosol Transmissible Diseases. The Employer does not provide employees with PPE on the Unit. Nurses do not have immediate access to PPE, including N- 95 respirators. The nurses frequently do COVID-19 swabs for pre-op screenings. California Code of Regulations, Title 8, Section 5193(d)(3)(E)(3) and 5193(i). Bloodborne Pathogens. Biohazard trash has not been removed since February 2021. There has been blood product waste in the dirty linen area since the unit was moved to the former L&D Unit. Complainant notes: BBP: Biohazard trash not emptied since February. No PPE on unit. Nurses do not have immediate access to PPE, including N95s. Nurses do COVID-19 swabs for pre op screenings. No lift equipment or means for single nurse to assist patients, pull up in bed or transfer to another bed/chair.
Alleged Hazards: 3,
Source: Osha.gov | Receipt Date: 2021-04-08
Alleged Hazards: 3,
Source: Osha.gov | Receipt Date: 2021-04-08
468
Covid-19 OSHA Complaint
2 years ago
Understaffed in the Covid floor, not getting breaks, not able to follow proper PPE protocols, exposing negative patients to Covid positive floors.
Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-09-16
Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-09-16
468
Covid-19 OSHA Complaint
2 years ago
The hospital did not provide adequate staff to monitor other staff donning of PPE. The staff of the Telemetry Unit had an inadequate and insufficient supply of PPE. A code blue was initiated on a COVID positive patient. There was insufficient PPE available for the staff and
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staff were subsequently exposed to COVID. Hospital management failed to address the urgent need for PPE, including respirators.
Source: Osha.gov | Receipt Date: 2020-10-16
Source: Osha.gov | Receipt Date: 2020-10-16
468
Covid-19 OSHA Complaint
2 years ago
The hospital failed to follow the ATD standard. Complainant was assigned a COVID-19 positive patient in the Emergency Department that did not go through the normal ER admission Process, not informed of COVID positive status, and not informed that patient was in respiratory distress while also being
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assigned to 3 other COVID positive patients.
Source: Osha.gov | Receipt Date: 2020-10-16
Source: Osha.gov | Receipt Date: 2020-10-16
468
Covid-19 OSHA Complaint
2 years ago
Hospital management failed to follow ATD standards by allowing a COVID positive patient in the Emergency Department wander the ER hallways without being placed in an isolation room. This exposed other patients and staff to COVID.
Source: Osha.gov | Receipt Date: 2020-10-16
Source: Osha.gov | Receipt Date: 2020-10-16
468
Recent Interesting Reports
Unordered package, Craig, CO, USA
15 hours ago •reported by user-hvffh693
I received a package I didn't order AND I received an email invoice for a computer software I can't find charges for (which account?) $300.00! Also, I tried to call customer service number on invoice and it was disconnected
1
Unordered Package, Albany, NY, USA
1 day ago •reported by user-gwxcb771
A small package was delivered to me with a purple plastic bottle inside. Was labeled but all in Chinese. Bottle half filled with unknown liquid. Did not order and not sure where came from.
a package I did not order, Boscobel, WI, USA
3 weeks ago •reported by user-hqjf6546
I received a package I did not order from
Rosewood P
2800 N Frankin Rd
Indianapolis, IN 46219
ugly black necklace inside the package
Rosewood P
2800 N Frankin Rd
Indianapolis, IN 46219
ugly black necklace inside the package
5
Got a package did not order, Wesley Chapel, FL, USA
2 weeks ago •reported by user-gcymm412
Did not order. Don’t even know what it is. Shows I owe fees now? WTH?
135
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
DGTGOODSGONS, Barletta, Province of Barletta-Andria-Trani, Italy
1 week ago •reported by user-hgfc4487
I placed an order online and my jacket didn't arrive I'll send them the email and they write to me that it arrived but not where
Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil, USA
2 days ago •source www.fda.gov
Recall notice
STOP CLOPEZ CORP is voluntarily recalling one lot of Schwinnng capsules to the consumer level. FDA analysis has found the Schwinnng products to contain Nortadalafil. Nortadalafil is an active drug ingredient known for the treatment of male erectile dysfunction. The presence of Nortadalafil in Schwinnng capsules makes
…
it an unapproved new drug for which the safety and efficacy have not been established and, therefore subject to recall. The product was distributed Worldwide via Amazon at www.amazon.com. To date, no adverse events have been reported.
The Schwinnng products contain Nortadalafil, which may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, adult males who use nitrates for cardiac conditions are most at risk.
This product is marketed as a dietary supplement for male sexual enhancement and is packaged and coded as follows:
SCHWINNNG Lot 2108 EXP 10/2024
STOP CLOPEZ CORP is notifying its customers by this press announcement of this recall release and is arranging for a return of all recalled products. Consumers that have a Schwinnng product that is being recalled should stop using and destroy / return if desired to STOP CLOPEZ CORP. Schwinnng products must include the blister pack foil (with any pills remaining) containing all lot codes and receipt of proof of purchase, and your return address.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Link to FDA Advisory
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: STOP CLOPEZ CORP
Brand name: Schwinnng
Product recalled: Herbal Dietary Supplement
Reason of the recall: Product is tainted with Nortadalafil
FDA Recall date: April 23, 2024
Source: www.fda.gov
The Schwinnng products contain Nortadalafil, which may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population, who are most likely to use this product, adult males who use nitrates for cardiac conditions are most at risk.
This product is marketed as a dietary supplement for male sexual enhancement and is packaged and coded as follows:
SCHWINNNG Lot 2108 EXP 10/2024
STOP CLOPEZ CORP is notifying its customers by this press announcement of this recall release and is arranging for a return of all recalled products. Consumers that have a Schwinnng product that is being recalled should stop using and destroy / return if desired to STOP CLOPEZ CORP. Schwinnng products must include the blister pack foil (with any pills remaining) containing all lot codes and receipt of proof of purchase, and your return address.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Link to FDA Advisory
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: STOP CLOPEZ CORP
Brand name: Schwinnng
Product recalled: Herbal Dietary Supplement
Reason of the recall: Product is tainted with Nortadalafil
FDA Recall date: April 23, 2024
Source: www.fda.gov
303
I never ordered these two health watches, New Jersey, USA
2 weeks ago •reported by user-mgnd9632
I received two health watches in the mail today..I never ordered these
272
Unwanted purchases, 2207 Summit Avenue, Union City, NJ 07087, USA
3 weeks ago •reported by user-pgjrm872
Do not want purchase not as described in website ! Need to return for refund!
2.8K
Unordered Package, 9208 Charles Smith Ave, Rancho Cucamonga, CA 91730, USA
1 week ago •reported by user-vqtpn585
I received a package that I never ordered. I don’t even know what the contents are - they are a pair of some sort of small silicone items. The return address on the package is:
Jerry Yasfbara
9208 Charles Smith Ave.
Rancho Cucamonga, CA 91730
It came …
Jerry Yasfbara
9208 Charles Smith Ave.
Rancho Cucamonga, CA 91730
It came …
USPS with tracking #92612927005455000751******
Please let me know if you have any questions or need more information.
I don’t believe I have any outstanding orders that I have not received.
Please let me know if you have any questions or need more information.
I don’t believe I have any outstanding orders that I have not received.
702
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