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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

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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Recent Interesting Reports

February 10, 2021 10:00 PM

“Company name: NDAL MFG INC
Brand name: ManukaGuard
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FDA Recall date: February 10, 2021
Recall details: NDAL MFG INC is voluntarily recalling one lot of Manukaguard Allercleanse, nasal spray to the consume... See Morer level. The Allercleanse nasal sprays have been found to be contaminated with yeast.

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Product was distributed Nationwide in the USA to 1 e-commerce website amazon.com, distributors and retail stores. NDAL MFG INC has notified its distributors and customers by e-mail followed by telephone and further email and has arranged for return/replacement etc. of all recalled products. 

Consumers/distributors/retailers that have product which is being recalled should stop using/return to place of purchase/discard/contact their doctor, etc., if they have not already done so. Consumers with questions regarding this recall can contact NDAL MFG INC by phone 1-800-916-1220 or e-mail address SUPPORT@MANUKAGUARD.COM, M-F 7:30 am to 4 pm PST.  Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

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Brand name: Apotex Corp.
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Reason of the recall: Packaging error resulting in incorrect dosage listed
FDA Recall date: February 03, 2021
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Health Hazard Assessment: Incorrect syringe barrel marking could lead to miscalculation and inaccurate dose administration to patients. In one recalled batch (batch CS008, strength 100 mg/mL), if a consumer used a 150 mg/mL concentration packaged in a barrel corresponding to a l00 mg/mL concentration, patients could receive 3.75 mg of Enoxaparin, instead of 3 mg of Enoxaparin. In another recalled batch (batch CT003, strength 120 mg/0.8mL), if a consumer used a 100 mg/mL concentration packaged in a barrel corresponding to a 150 mg/mL concentration, patients would receive 2 mg of Enoxaparin rather than 2.5 mg of Enoxaparin. Accidental overdosage following administration of enoxaparin sodium injection may lead to bleeding complications. Alternative, if the dose administered is less than prescribed, the patient may be subject to developing some blood clotting conditions.

Enoxaparin Sodium injection is indicated for the prophylaxis of deep vein thrombosis (DVT), which may lead to pulmonary embolism (PE), Treatment of Acute Deep Vein Thrombosis, prophylaxis of ischemic complications of unstable angina and non-Q-wave myocardial infarction, when concurrently administered with aspirin and Treatment of Acute ST-Segment Elevation Myocardial Infarction.

The affected Enoxaparin Sodium Injection, USP can be identified by NDC numbers stated on carton and label of the product.

Product: Enoxaparin Sodium Injection, USP
Batch #: CS008
Strength: 100 mg/mL
Syringe Barrel Measurement Markings: 100 mg/mL
Pack Size: 10 x 1mL Single Dose Syringes
NDC NumberOn Carton: 60505-0795-4
NDC Number On label: 60505-0795-1
UPC Code on Carton: 360505079544
UPC Code on label: (01)10360505079510

Product: Enoxaparin Sodium Injection, USP
Batch # : CT003
Strength: 120 mg/0.8mL
Syringe Barrel Measurement Markings: 150 mg/ mL
Pack Size: 10 x 0.8 mL Single Dose Syringes
NDC NumberOn Carton: 60505-0796-4
NDC Number On label: 60505-0796-0
UPC Code on Carton: 360505079643
UPC Code on label: (01)10360505079602

The two (2) affected batches of Enoxaparin Sodium Injection, USP were distributed by Apotex nationwide in the USA to Wholesalers and Warehousing Chains. Apotex Corp. is currently notifying its affected direct account Wholesalers and Warehousing Chains, via mail (FedEx Standard Overnight) by mailing a recall notification letter and is arranging for return of all recalled product.

Check the full recall details on fda.gov

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New Jersey, USA

January 25, 2021 11:34 PM

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Crewe, VA, USA

January 29, 2021 12:23 AM

“I reported earlier today that I received the second dose of Pfizer at work Wednesday by CVS, I am now broken out with a wicked rash on both legs, and feet. It’s itchy and looks horrible. Never had a rash like this.

_______________________________

Previous Report: Jan 28, 2021
Took the second... See Moredose of Pfizer at work yesterday given by CVS. CVS worker was good with a needle did not even feel the shot go in-she has that skill mastered. Slight burning for a few moments after potion entered bloodstream. Mildly tender arm- left upper arm where vaccine was given. It was mild enough I did not have to take any PRNs for pain or discomfort. Next morning after vaccine ( this AM) I felt a bit sluggish-no energy-arm still mildly sore-still not having to take a PRN for pain. Not sure if it was from the vaccine or me working 14 hours day before-just put it this way-I work a lot of 14 hour days and was not that sluggish feeling in the AM. Other than that I'm good-no headache, no dizziness, I have been monitoring my temp and I have not had one, my temp runs around 97.3 etc..We are tested for COVID where I work every week due to having a outbreak in our geriatric hospital on all floors killing many of the geriatric patients, staff shortage, nurses, doctors, sick with COVID-so far I am one of only a few staff that has not tested positive for COVID. If I have any symptoms in the next few days from the vaccine I will report. Stay safe!! See Less
Reported By SafelyHQ.com User

February 4, 2021 9:46 AM

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