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Food City, 429 University Dr, Prestonsburg, KY 41653, USA

Total all time reports:  1
Latest report: April 28, 2020 12:00 PM
Supermarket employee tests positive for COVID -19, Food City, 429 University Dr, Prestonsburg, KY 41653, USA

Supermarket employee tests positive for COVID -19

April 28, 2020 12:00 PM

“A Food City employee at the Prestonsburg, KY location has tested positive for COVID-19. The employee last worked on Saturday, April 25. If you visited the supermarket during that time, please report it and any other location that you visited.



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

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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.

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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.

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

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Check the full recall details on fda.gov

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Check the full recall details on fda.gov

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

Check the full recall details on fda.gov

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