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Covid-19 OSHA Complaint, Vons, 1702 Garnet Avenue, San Diego, California 92109, USA
3 years ago
1702 Garnet Avenue, San Diego, 92109 California, United States
T8 CCR 3203(a)(4) Employer is not adhering to Public Health Department & CDC guidelines during the pandemic such as not maintaining distancing amount employees and customers, no hand sanitizers available for employees, no 6 -feet space between registers.
T8 CCR 3241(c) Wood pallets are stacked on edge in the corridor not secured.
T8 CCR 3272(b) Material stacked in walkway near the break room, walkway less than 24 inches.
T8 CCR 3362(g) Water intrusion at ceiling various areas of the store; stains on the ceiling, concern for mold.
Alleged Hazards: 4, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-07-23
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Since that notification, we have continued to monitor device performance through post market surveillance, investigated every event reported and evaluated potential root cause of these events. Megadyne recently received a report of pediatric use that included a serious 3rd degree patient burn. We are providing this additional broad public communication to increase awareness that MEGADYNE™ MEGA SOFT™ Universal and Universal Plus products should not be used for patients under the age of 12 years.
The list below contains the specific product and codes in scope.
- Product Name: MEGADYNE™ MEGA SOFT™ Universal Patient Return Electrode, Product Code: 0845, UDI-DI: 10614559103906.
- Product Name: MEGADYNE™ MEGA SOFT™ Universal Dual Patient Return Electrode, Product Code: 0846, UDI-DI: 10614559104248.
- Product Name: MEGADYNE™ MEGA SOFT™ Universal Plus Patient Return Electrode, Product Code: 0847, UDI-DI: 10614559104842.
- Product Name: MEGADYNE™ MEGA SOFT™ Universal Plus Dual Patient Return Electrode, Product Code: 0848, UDI-DI: 10614559104859.
Customers should review and follow the instructions provided in the December 2023 recall notification (link given below). Mega Soft Universal and Universal Plus Reusable Patient Return Electrodes pads may continue to be used for patients over 12 years of age.
Confirm that personnel using the Mega Soft Universal and Universal Plus pads understand the intended use is changing to patients aged 12 years and older and have stopped using the pads on patients under the age of 12 years. Hospitals using this product should confirm receipt of the recall notification using the business reply form provided with the initial recall notification.
In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Megadyne Medical Products, Inc.
Brand name: Megadyne
Product recalled: Mega Soft Universal and Universal Plus Reusable Patient Return Electrodes
Reason for the recall: Limit use to patients aged 12 years or older.
FDA Recall date: February 29, 2024
Recall link of December 2023: jnjmedtech.com
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