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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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Nebraska Department of Correctional Services, 801 W Prospector Pl, Lincoln, NE 68522, United States

Total all time reports:  1
Latest report: April 30, 2020 12:00 PM
Another Nebraska Department of Correctional Services employee tests positive for COVID-19, Nebraska Department of Correctional Services, 801 W Prospector Pl, Lincoln, NE 68522, United States

Another Nebraska Department of Correctional Services employee tests positive for COVID-19

April 30, 2020 12:00 PM

“On Wednesday April 29, officials said another staff member at the Nebraska Department of Correctional Services (NDCS) has tested positive for COVID-19. This is the fourth employee with NDCS to receive a positive result. No inmates have tested positive for COVID-19.

Source: ketv.com See Less
Reported By SafelyHQ.com User

Related Reports

July 12, 2020 12:00 PM

“Three Port Authority employees recently tested positive on July 4 and one tested positive on Wednesday for Covid-19. This brings positive cases to the total number of employees to 21.

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Reported By SafelyHQ.com User

Employee test positive for Covid-19, Dairy Queen Grill & Chill, 2719 Charity St, Abbeville, LA 70510, USA

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Possible Covid-19 outbreak, Duke's Seafood, 2516 Alki Ave SW, Seattle, WA 98116, USA

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July 12, 2020 12:00 PM

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Employee test positive for Covid-19, East 55th on the Lake, 5555 N Marginal Rd, Cleveland, OH 44114, USA

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“An employee at e55 on the Lake restaurant tested positive for COVID-19. The employee last reported to work on Tuesday, July 7.

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Recent Interesting Reports

April 29, 2020 7:00 PM

“Company name: CME America
Brand name: CMEAmerica BodyGuard
Product recalled: Infusion pumps and infusion sets
Reason of the recall: pumps may not deliver fluid at the accuracy specified in the instructions for use and infusion sets may under-deliver fluids
FDA Recall date: April 29, 2020
Recall ... See Moredetails: CME America, a wholly owned subsidiary of BD (Becton, Dickinson and Company), a leading global medical technology company, today issued the following update regarding two previously announced voluntary recalls, one related to all models of CMEAmerica BodyGuard® infusion pumps (FDA Recall Number: Z-1474-2020) and the other related to one of the device's infusion sets (FDA Recall Number: Z-1442-2020). Both previously announced recalls have now been designated as Class I recalls by the U.S. Food and Drug Administration (FDA), which means the FDA believes that there is a reasonable probability that use of the recalled product(s) will cause serious adverse health consequences or death.

CME America previously notified customers affected by each recall and provided guidance on the potential impact to device performance when the affected products were used. Today, the company has issued an updated customer letter with additional guidance and to inform customers of the decision to suspend distribution of the BodyGuard® infusion pump system and to remove all existing products from the U.S. market.

The following is a summary of each individual product recall details:

CMEAmerica BodyGuard® Infusion Pump Recall

Details On Jan. 6, 2020, the company initiated a voluntary recall to notify customers of certain scenarios where pumps may not deliver fluid at the accuracy specified in the instructions for use that could result in a slower than expected delivery of medication (under-infusion), and/or faster than expected delivery of medication (over-infusion). Results indicate that pumps may have a delivery inaccuracy of up to ~13%. To date, no reports of patient injury has been received related to this previously announced voluntary recall. CME America has assessed the potential risks associated with the issues outlined in the initial voluntary recall and determined that the BodyGuard® infusion pump may continue to be used in certain situations in accordance with the Operator's Manual and the additional mitigations outlined in the updated customer letter until the pumps have been removed from the market.

To ensure customers retain access to critical medical equipment, particularly as the COVID-19 pandemic continues to evolve in the United States, CME America will implement a phased market removal and will continue to support the following activities in order to help limit clinical disruption and maintain patient focus during the COVID-19 pandemic: Use of products in the field in accordance with the Operator's Manual and the additional mitigations outlined in the updated customer letter; Product service and repair activities at CME America and Authorized Service Depots; and Supply of infusion sets and accessories to support the infusion pumps remaining in the field.

The BodyGuard® infusion pump is designed to deliver fluids or medications into a patient's body in controlled amounts. The pump administers fluids through an infusion tubing set into a patient's vein or through other cleared routes of administration. The system is intended for patients who require maintenance medications, PCA therapy, parenteral nutritional fluids, and general IV fluid therapy in hospital and home care environments. Typical applications for the BodyGuard® infusion pumps include but are not limited to chemotherapy, pain management, TPN, enteral nutrition fluids and antibiotics.

The recall and market removal affect approximately 28,400 devices, including all models of BodyGuard® infusion pumps listed below. These devices are primarily used in outpatient settings.
- BodyGuard 121
- BodyGuard 323
- BodyGuard 545*
- BodyGuard 575*
- BodyGuard 545 ColorVision
- BodyGuard 575 ColorVision
- CMExpress

*Note: These two pump models were inadvertently left out of the initial customer notification

CMEAmerica BodyGuard® Microset Infusion Set Recall

Details On Sept. 16, 2019, the company initiated a voluntary recall to notify customers that certain lots of BodyGuard® Microset infusion sets, when used with the BodyGuard® infusion pump, may under-deliver fluids up to 50% at the highest flow rates. At the time of the recall, CME America informed customers in the recall announcement to discard all remaining inventory of the infusion sets (Catalog #A120-003XYVA) and committed to reimbursing impacted customers. To date, no reports of patient injury has been received related to this previously announced voluntary recall. CME America immediately stopped shipments of the affected infusion sets. This FDA classification does not change the previous guidance provided in the company's September recall announcement to customers. Affected products include:

CMEAmerica BodyGuard® Microset, Catalog #A120-003XYVA.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

May 26, 2020 9:34 PM

“Wifey wants to thank you for the raw chicken sandwich and upcoming bout of diarrhea. PukeCity See Less
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Peaceful Protest, Long Island City, Queens, NY, USA

Long Island City, Queens, NY, USA

June 6, 2020 1:16 PM

“Peaceful Black Lives Matter protest at Gantry Plaza See Less
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April 12, 2020 12:00 PM

“Details: A sixth employee at a ShopRite in the Hudson Valley has tested positive for the novel coronavirus (COVID-19).
The store is asking colleagues who may have been in close contact with that person to self-quarantine for a period of 14 days

Report: 4/10/2020
Source: dailyvoice.com See Less
Reported By SafelyHQ.com User

Allergic to Meat and Given a Chicken Quesadilla, Taco Bell, 2410 East Rand Road, Arlington Heights, IL, USA

Symptoms: Nausea
Taco Bell, 2410 East Rand Road, Arlington Heights, IL, USA

June 25, 2019 10:54 PM

“I am a vegetarian and ordered food. I was shell shocked after i received chicken ... See More-link" href="https://safelyhq.com/product/quesadilla#scroll" title="Product: Quesadilla">quesadilla and unknowingly i took a bite of it. On checking with the manager he told sorry and said he is not responsible for his employee mistake and said he is not sure on how to comaint this to a higher level. Also he said if anything happens to me i should come back and then sue the company.i am allergic to meats please let me know how to take this. I am feeling so pukish See Less
Reported By SafelyHQ.com User

July 7, 2020 3:00 PM

“Company name: Mylan Institutional LLC
Brand name: Mylan
Product recalled: Daptomycin for Injection
Reason of the recall: Presence of particulate matter
FDA Recall date: July 07, 2020
Recall details: Mylan N.V. (NASDAQ: MYL) today announced that its U.S.-based Mylan Institutional LLC business is ... See Moreconducting a voluntary nationwide recall to the consumer level of one lot of Daptomycin for Injection, 500 mg/vial due to the presence of particulate matter found in one single-dose vial manufactured by Mylan Laboratories Limited’s Specialty Formulation Facility. To date, Mylan has not received any reports of adverse events related to this recall.

Intravenous administration of a solution containing visible particulates could lead to serious adverse events including, but not limited to, local irritation, vasculitis/phlebitis, antigenic or allergic reactions, and microvascular obstruction, including pulmonary embolism. This batch was distributed nationwide to wholesalers and retail pharmacies between April 2020 and May 2020. The recalled batch is as follows:

- NDC #: 67457-813-50
- Material Description: Daptomycin for Injection
- Strength: 500 mg/vial
- Size: 20 mL vial
- Lot No: 7605112
- Expiry: October 2021

Daptomycin for injection is an injectable antibacterial indicated for the treatment of complicated skin and skin structure infections (cSSSI) and staphylococcus aureus bloodstream infections (bacteremia) in adult patients.

Mylan is notifying its distributors and customers by letter and is arranging for return of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop use/further distribution or dispensing.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

Chicken from Costco is almost raw, Costco Wholesale, 16580 NW 59th Ave, Hialeah, FL 33014, United States

Costco Wholesale, 16580 NW 59th Ave, Hialeah, FL 33014, United States

May 6, 2020 9:35 PM

“Translation:
Honestly, I love Costco, and I'm not trying to put any employee in a bad light, especially in the chicken-rotisserie area. I have a picture of how red hot it is on a piece of ... See Morebtn-link" href="https://safelyhq.com/product/meat#scroll" title="Product: Meat">meat and blood on the bones. Chickens need more fire and cooking.

Original:
Con sinceridad, amo Costco, y no trato de poner en mal a ningun empleado en especial la zona de los asadores de pollo. Tengo la foto lo rojo vivo que esta en una parte de la carne y sangre en los huesos. Los pollos necesitan mas fuego y cocimiento. See Less
Reported By SafelyHQ.com User

Hardee's, Army Post Road, Des Moines, IA, USA, Hardee's, Army Post Road, Des Moines, IA, USA

Symptoms: Other
Hardee's, Army Post Road, Des Moines, IA, USA

June 5, 2020 8:07 AM

“Foreign objects in coffee. Looked like burger from nose. See Less
Reported By SafelyHQ.com User

April 12, 2020 12:00 PM

“Details: A Bojangles' employee here tested positive for COVID-19, prompting the fast food restaurant to close temporarily and send some 20 other workers home to self quarantine.

Report: 4/08/2 ... See More020
Source: greensboro.com
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Reported By SafelyHQ.com User

March 18, 2020 2:42 PM

“An employee at a Waffle House has tested positive for coronavirus, according to the restaurant. That employee works at the restaurant at 1849 Marietta Highway in Canton, Georgia and the location is temporarily closed.

"During the restaurant closure, we sanitized the restaurant thoroughly, using ... See Moremethods specifically designed to clean and disinfect," said the Waffle House Director of Public Relations Njeri Boss (...).

Waffle House said the employee last worked on March 1 and that the 12 co-workers who worked with that person were instructed to self-quarantine at their homes through Saturday, March 14.

Source: 11alive.com
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Reported By SafelyHQ.com User