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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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Freedom Square of Seminole, 7800 Liberty Ln, Seminole, FL 33772, USA

Total all time reports:  1
Latest report: April 20, 2020 12:00 PM
58 people at Seminole nursing home test positive for COVID-19, Freedom Square of Seminole, 7800 Liberty Ln, Seminole, FL 33772, USA

58 people at Seminole nursing home test positive for COVID-19

April 20, 2020 12:00 PM

“39 patients & residents and 19 employees at Seminole nursing home have recently tested positive for COVID-19.

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

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Recent Interesting Reports

July 6, 2020 11:33 AM

“not a good look... I was served pretty much raw chicken 🤢🤮 See Less
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July 13, 2020 11:30 PM

“The FSA announced the recall of various brands of raw dog food products containing beef by Benyfit Natural Pet Food because of the potential to be contaminated with Salmonella.

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046-076. 16 March 2021 / 046-083. 23 March 2021 / 046-093. 2 April 2021 / 046-100. 9 April 2021

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The Company has received reports of adverse reactions. Pet parents that have questions or would like to report adverse reactions should call 888-569-6828, Monday through Friday, 8 a.m. – 5 p.m. ET or email anytime at info@naturalbalanceinc.com.

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April 12, 2020 12:00 PM

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February 23, 2020 4:39 AM

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Protests, Austin, TX, USA

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July 8, 2020 4:00 PM

“Company name: CME America
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FDA Recall date: July 08, 2020
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This testing revealed that some infusion sets do not meet the ±5% delivery accuracy for the system or the ±13% accuracy identified in the earlier recall notification (bd.com Therefore, the use of the pump system potentially could cause over-infusion or under-infusion of therapy and patient harm. Based on those test results CME America is providing additional information and customer actions regarding its previous recall to include all infusion sets used with the BodyGuard® infusion pump distributed beginning May 2016.

CME America has defined four categories of impacted infusion sets based on delivery inaccuracy variability, two of which (Category A and B) can continue to be used in accordance with the instructions in the recall letter (bd.com CME America also announced on April 27, 2020, the decision to suspend distribution of the BodyGuard® infusion pumps and to remove all existing products from the U.S. market. CME America will work with customers to address the latest expanded infusion set recall and will continue to maintain continuity of care during the COVID-19 pandemic. Until such time that the BodyGuard® pumps have been removed from the market, CMEA will supply accessories and infusion sets in "Category A" and "Category B" to support the infusion pumps, and customers can continue to use the products in accordance with the Operator's Manual and the additional mitigations outlined in the customer letter.

Affected Product Types:

- BodyGuard BodySet
- BodyGuard Microset with Needleless Adaptor
- BodyGuard Microsets
- BodyGuard Microset w/ Non-Vented Spike Connector
- BodyGuard set with Female Luer
- BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer
- BodyGuard Microsets with Filter
- Standard BodySet with Needleless Connectors
- BodyGuard Microset with Filter and Manual Priming Valve
- CMExpress Microbore Sets
- BodyGuard Microset with Male Luer Connectors
- CMExpress Needleless Y Site Microbore Set

Check the full recall details on fda.gov

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May 26, 2020 3:35 PM

“Thanks for my raw chicken ? See Less
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April 23, 2020 8:51 AM

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May 26, 2020 9:34 PM

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