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The Shell House Restaurant, 8 Gateway Blvd W, Savannah, GA 31419, USA

Latest report: June 23, 2020 12:00 PM
#coronaviruscovid19 #8gatewayboulevardwest #savannah #georgia #unitedstates
XR

Employee test positive for COVID-19

1 year ago

An employee at The ShellHouse Restaurant in Savannah has tested positive for COVID-19 on June 18. If you visited the restaurant recently, please report it and any other location that you visited.

Source: wtoc.com See Less
284


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Recent Interesting Reports

I bought these as a special gift for my little Maltese cross. Last night I gave her one. This morning I gave her another one. She’s been non stop puking, trying to poo.
Very uncomfortable.

The only thing different in her diet was introducing these treats.

When... See More I pulled the treats out to read the label today after seeing her like this. She had no interest in the treats. Like she is aware that this is what’s hurting her.
I bought them at the superstore location on Hardin street in Fort Mcmurray Alberta.

After researching them. I feel like they need to be pulled from shelves.

If someone can go to jail for kicking a dog a store and a product owner should also be charged with hurting and animal.
I hope my dog will be okay. And I had kept my bag as evidence in a area closed off to public or any animal.

Thank you. | Symptoms: Vomiting
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12


ET
ethelt9
I only give my dog fresh fried fish, scrap stuff, I fry myself and when I make meat for my family I also make meat for my dog, I have never understood why we should even buy prepackaged treat's for our fur babies, besides it's more expensive and got lots of fillers that have nothing to do with carnivore eating mammals. I hope you get to the bottom of what caused your baby to fall ill after consuming those treats.
Reply 2 weeks ago
Taro Pharmaceuticals U.S.A., Inc. (“Taro” or the “Company”) is voluntarily recalling one (1) lot of Clobetasol Propionate Ointment USP, 0.05% packaged in 60 g tubes, to the consumer level. This recall ONLY applies to tubes labeled with “Lot AC13786” and “Exp Dec 2022”. No other lots of... See More this product are impacted.

Lot AC13786 is being recalled due to the presence of Ralstonia pickettii bacteria (“R. pickettii”), which was discovered by the manufacturer through routine testing. R. pickettii is present in the natural environment (soil, water) and for healthy individuals with intact skin, is unlikely to cause any localized or systemic infections. However, for individuals who are immunocompromised, or whose skin is not intact (i.e. sunburn, psoriasis, abrasions), there is a reasonable possibility that systemic infections may occur if the product is contaminated with R. pickettii due to the presence of the corticosteroid component which enhances absorption of the ointment. If this bacterium is circulating in the human blood stream it can cause life-threatening, invasive infections such sepsis, pneumonia, meningitis, inflammation of the bone or bone marrow, and infection in the joint fluid and joint tissues.

To date, Taro has not received any adverse event reports related to this lot.

The one (1) lot being recalled is as follows:

Lot # AC13786
Amount: 96 units
Expiration Date: December 2022

Clobetasol Propionate Ointment USP, 0.05% is indicated for the relief of inflammatory and pruritic manifestations of corticosteroid responsive dermatoses and is packaged in 60 g aluminum tubes with polypropylene puncture-tip caps. Each 60 g tube is labeled to indicate the name of the product, Clobetasol Propionate Ointment USP, 0.05% and the NDC # 51672-1259-3 (see image of container label below). The Lot Number and Expiration Date are displayed on the bottom of each tube and the end flap of the product carton.

Ninety-six (96) units of Lot AC13786 were distributed to two wholesale distributors in the U.S. market between November 16 and December 6, 2021. These two wholesale distributors may have further distributed this lot to their retail customers for prescription dispensing to patients who were prescribed Clobetasol Propionate Ointment USP, 0.05%, 60 g.

Retail customers that have any quantities of Lot AC13786 which is being recalled, should stop distribution and return any unsold units to their wholesaler. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

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

Company name: Taro Pharmaceuticals USA, Inc.
Brand name: Taro
Product recalled: Clobetasol Propionate
Reason of the recall: Presence of Ralstonia pickettii bacteria
FDA Recall date: December 30, 2021

Check the full recall details on fda.gov

Source: FDA
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112


I turned on the water and small black spots appeared as I was pouring it in a white cup. Then the water when I turned it on a little bit looked murky white. See Less
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Oscor Inc. is voluntarily recalling 14 lots of Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 down to the user level. The Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 have been found to have increased risk of the hub cap and seal... See More on the proximal end of the device handle detaching during use.

RISK STATEMENT: The Destino Twist 14T Model DST1405525 & Guidestar 14F Model D141103 detachment of the hub cap and seal could lead to bleeding at the proximal end of the device and/or air embolism for the patient during intracardiac, renal or other peripheral placements procedures.

Oscor Inc. has reported two (2) Medical Device Reports to the FDA related to detachment of hub cap and seal on the proximal end of the device handle. The recall is limited to the two model numbers and lot numbers outlined above. There are no other recalls associated with this product.

PRODUCT INFORMATION: The product is steerable guiding sheath intended for the introduction of diagnostic and therapeutic devices into the human vascular, including but not limited to intracardiac, renal or other peripheral placements; it cannot be use for neural placements. The product is provided sterile, one unit per pouch / tray for details and can be identified on the printed labeling with the information below (1, 2, and 3).

The affected Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 were distributed Worldwide to distributors and hospitals from June 8, 2021 to November 30, 2021.

Recalled Product Impacted (1)

- Destino Twist 14F (DST1405525). UDI Number: 885672011123. Lot Number: PQOC13475. Expiration Date 10-01-2021. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14073. Expiration Date 11-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14072. Expiration Date 10-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14071. Expiration Date 10-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13834. Expiration Date 09-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13828. Expiration Date 09-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13827. Expiration Date 08-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12995. Expiration Date 07-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12632. Expiration Date 07-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12633. Expiration Date 07-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12345. Expiration Date 06-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12330. Expiration Date 06-01-2025. Packaging State Type: Sterile.

Destino 14F Twist Model (2)

Product: Destino Twist 14F
GTIN (Unit): 00885672011123
Model: DST1405525
Sheath & Dilator: S55CM D73CM
French Size: 14F
Quantity: 6 Units

Guidestar 14F - Model (3)

Product: Guidestar 14F
GTIN (Unit): 00885672010911
Model: D141103
Sheath & Dilator: S71CM D89CM
French Size: 14F
Quantity: 543 Units

Company name: Oscor Inc.
Brand name: Oscor
Recalled: Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 steerable guiding sheath
Reason of the recall: Hub cap and seal on the proximal end of the device handle may detach during use
FDA Recall date: January 12, 2022

Check the full recall details on fda.gov

Source: FDA
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111


Package ID: 0652097001
Delivery conf at Teterboro: 92748909840515553021375525
Ordered small package that has been sitting at Teterboro since 12/8/21…it’s been a month and still not delivered. This is ridiculous!!!!! See Less
5.6K


I mailed a package from Lake Luzerne, NY on 12/8/21 and tracking states it arrived in Teterboro, NJ on 12/12/21. There are no further updates other than "in transit" and the package has not been delivered. On their website, it states this facility is permanently closed! Tracking... See More #9505 5124 5581 1342 2096 34 See Less
5.6K


World Health Products, llc. of Monroe, CT is recalling Jetfuel Diuretic UPC 859613000859, because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.

The GAT Sport Jetfuel... See More Diuretic was distributed thru the GAT Sport online store, Amazon and “Nationwide” retail stores. The recalled products bear the following lot code and Expiration Date information:

Brand: GAT Sport / Jetfuel Diuretic
Product: Jetfuel Diuretic
Size: 90 ct Bottle
Lot # 2003609
Exp. Date: 6/2023

Brand: GAT Sport / Jetfuel Diuretic
Product: Jetfuel Diuretic
Size: 90 ct Bottle
Lot # 2003610
Exp. Date: 5/2023

The lot code and expiration date are located on the bottom of the container, in bottom center of the panel, as pictured below.

This recall is being initiated because the Medium-Chain Triglycerides (MCT) oil powder ingredient contains an undeclared milk allergen.

This recall is being carried out with the knowledge of the Food and Drug Administration.

To date there have been no reports of illness involving the products addressed in this recall.

Customers with a milk allergy or sensitivity who have purchased the affected product are urged not to consume it and dispose of it or return it to the point of purchase.

In case you are experience harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: World Health Products, LLC
Brand name: GAT Sport Jetfuel Diuretic
Product recalled: Diuretic
Reason of the recall: May contain undeclared milk
FDA Recall date: January 06, 2022

Check the full recall details on fda.gov

Source: FDA
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111


I am the employee, I was exposed to someone who tested positive for Covid outside of the Amazon facility. I started to have all the symptoms of Covid on or around the 6th - 7th of January 2022. I looked for a test for about a week... See More or so, and finally found somewhere to get a test, and today I received my results today that I am positive for Covid. See Less
423


ALDI is voluntarily recalling Pure Being Cat Advent Calendars and Pure Being Dog Advent Calendars as a precautionary measure due to a potential choking hazard. After receiving a small number of customer complaints and discussion with the supplier, ALDI immediately removed the affected products from stores. The... See More affected products are:

- Pure Being Cat Advent Calendar (5.15 oz Box). UPC: 4099100267754. Best If Used By: All
- Pure Being Dog Advent Calendar (5.15 oz Box) UPC: 4099100267747. Best If Used By: All

No other ALDI products are affected by this recall.

ALDI takes the safety and integrity of the products it sells seriously. If customers have product(s) affected by this voluntary recall, they should discard it immediately or return it to their local store for a full refund.

Customers may contact Pet Brands Products’ Customer Service at 866-396-3647 for more information.

Company name: ALDI
Brand name: Pure Being
Product recalled: Advent Calendars for Cats and Dogs
Reason of the recall: Potential choking hazard
FDA Recall date: January 04, 2022

Check the full recall details on fda.gov

Source: FDA
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111


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