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Covid-19 OSHA Complaint, GGG Demolition Inc, 2850 Logan Avenue, San Diego, CA 92113, USA
3 years ago
2850 Logan Avenue, San Diego, 92113 California, United States
T8 CCR 1523(a) Inadequate lighting in crawlspace - I small light. T8 CCR 1526(d) Portable restroom are not properly cleaned and disinfected. T8 CCR 1527(a)(1)(D) No paper towel with the hand-washing facilities. T8 CCR 1529(d)(2) Tears in the asbestos abatement containment area plastic is not repaired. T8 CCR 1952(e)(2)(E) Employees are in a confined space (crawlspace under classrooms) without adequate ventilation. T8 CCR 2500.7(a) Household two-prong extension cords in use for saw-all, no three-prong cords. T8 CCR 3203(a)(6) Employer does not enforce COVID-19 guidelines including mask wearing.
Alleged Hazards: 7, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-26
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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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