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Papa John's Pizza, Solomons, MD 20688, USA
Latest report: July 2, 2020 12:00 PM
QJ
Employee test positive for Covid-19
1 year ago
An employee at Papa Johns in Solomons tested positive for COVID-19
Source: smnewsnet.com See Less
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7 employees tested positive for Covid-19 at Precision Aircraft Solutions in Washington County. Investigation Start Date: 18-11-2021, with the most recent onset of: 12-11-2021 New Cases of: 7
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58 employees tested positive for Covid-19 at Roseburg Forest Products: Riddle Plywood in Douglas County. Investigation Start Date: 24-05-2021, with the most recent onset of: 15-11-2021 New Cases of: 58
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Pfizer Reaction, White Plains, MD, USA
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About 6 minutes after taking second pfizer dose, I began to sweat, blood pressure dropped, nausea set in and almost lost consciousness a couple of times. A nurse and a doctor stayed with me and offered some water. That didn't help ad after about an hour, I... See More was taken by ambulance to emergency room and treated with fluids and anti-nausea feeds. About 5-6 hours later I began to feel better and went home. | Symptoms: Nausea See Less
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About 6 minutes after taking second pfizer dose, I began to sweat, blood pressure dropped, nausea set in and almost lost consciousness a couple of times. A nurse and a doctor stayed with me and offered some water. That didn't help ad after about an hour, I... See More was taken by ambulance to emergency room and treated with fluids and anti-nausea feeds. About 5-6 hours later I began to feel better and went home. | Symptoms: Nausea See Less
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Power Outage, Nottingham, MD, USA
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A Wednesday afternoon power outage has left several residents and businesses without power near the Dunfield and Belmont communities.
The outage was reported at just before 3:30 p.m. Initial reports indicate that nearly 2,500 residents are currently without power.
Source: nottinghammd.com
Source publication date: 2021 11 10 See Less
258
Covid-19 OSHA Complaint, Whitewood Assisted Living, 112 Collier Road, GRASONVILLE, MD, 21638, USA
1 month ago
Possibly employees are exposed to COVID-19 where personal protective equipment (PPE) was not provided. Possibly employees are exposed to COVID-19 where chemicals used for disinfecting was not provided.
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Vaccine side effects, Bel Air, MD, USA
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I have neuropathy pain and numbing in my feet and legs. Fatigue, light headed, runny nose, headaches almost daily, and joint pain since receiving my first phizer vaccination shot. My heart had a strong fluttering sensation within the first week and I couldn't get up at the... See More time while sitting on the floor with my little girl. It has only been a month and I do not believe how much information is on here showing that so many others are struggling like I am. This is terrible! | Symptoms: Other, Headache, Fatigue, Lightheaded, Joint Pain See Less
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Recent Interesting Reports
NJ post office is a ‘black hole’, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
4 weeks ago
On 9-24-21 I valued package was returned using Pitney Bowes shipping label provided by the merchant (American Mint). It was dropped off at the USPS store in Daytona Beach, picked up by Daytona Beach Post Office on 9-28-21 and retrieved from that Post office by Newgistics (Pitney... See More Bowes) on 9-30-21. On 10-4-21 it arrived and was dispatched from sorting at the Monroe Township, Middlesex County, New Jersey Post Office. Since then it is missing, in a black hole, unable to be found. This is a shame since this is a product scammed to my mother (senior of 86) who followed every step to have her $149.99 from American Mint and now can not receive her money back since the company has not received the product back. Please address this issue to return what is rightfully my mother's. This is a shame.
Pitney Bowes Returns
Parcel Return Service 56901
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5.4K
FOR IMMEDIATE RELEASE – December 1, 2021 – Princeton, NJ, Sandoz Inc. (“Sandoz”) is initiating a recall of one lot (SAB06761A, Exp 04/2023) of Enoxaparin Sodium Injection, USP 40 mg/0.4 mL Single-Dose Syringes to the consumer level. A portion of lot SAB06761A experienced a temperature excursion during... See More shipment. Enoxaparin Sodium for Injection Lot SAB06761A was shipped to customers in the months of September and October 2021.
The exposure to higher temperatures may have significantly impacted the recalled product’s (lot SAB06761A) effectiveness and thus there may be reasonable probability of risk for patients with health conditions that the product is intended to treat. Such patients could be at risk for blood clots blocking blood vessels, an artery, or traveling to other tissues or organs causing pain, swelling, stroke, clots to the lung or death as a result of the underlying condition. To date, Sandoz has not received any reports of adverse events or injuries related to this recall.
The product is used for prevention of deep vein thrombosis (DVT) a condition that occurs when a blood clot forms in a deep vein, usually in the legs that can occur after surgeries or in patients with restricted mobility during illness; or prevention of complications associated with heart attacks. The product is packaged in cartons containing ten 0.4 mL syringes, NDC 0781-3246-64. Enoxaparin Sodium Injection was distributed Nationwide in the USA to wholesalers and retailers.
Product Name: Enoxaparin Sodium, Injection, USP 40mg/0.4 mL
NDC Number: 00781-3246-64
Lot Number: SAB06761A
Expiration Date: 04/2023
Date of Manufacture: 05/26/2021
Please note: this recall is specific to only one batch (SAB06761A) of Enoxaparin Sodium Injection, USP 40 mg/0.4 mL and does not apply to any other strengths of Sandoz Enoxaparin Sodium Injection, USP or to other lots of the 40 mg/0.4 mL SKU.
Any product returned that is not associated with this recall will be destroyed and no credit issued.
Company name: Sandoz, Inc.
Brand name: Sandoz
Product recalled: Enoxaparin Sodium Injection
Reason of the recall: Exposure to high temperatures may have impacted product effectiveness.
FDA Recall date: December 02, 2021
Check the full recall details on fda.gov
Source: FDA See Less
102
Usually is fine. Not this time. I decided to burn Nag Champa incense to meditate. As I was meditating, our dog started sniffling and then began throwing up large amounts of mucous. Her lips were swollen and pulled back slightly. She is ok now, but I've never... See More experienced anything like this using incense before this happened. I often use it for meditation. I called the vet who confirmed this is an allergic reaction and they informed me to monitor her and ensure she is safeand healthy, not vomiting anymore. They instructed me to open all the windows and doors, turn on ceiling fans,and run the furnace heat to pull remaining particulate into the HEPA filter on the furnace and then to replace the filter tomorrow to ensure it doesn't just recirculate the particulate if any happens to get through. Also said to wash hard surfaces in the room it was burned on and vacuum up any furniture,carpet, or rugs there to remove any settled particulate. I'm not sure what went wrong here. I've never had this happen with her or any other dog when burning this.
But even I am sniffling and nauseous after having burned it and my throat is sore. I took benedryl to
prevent an attack in me personally.
Product:
Nag Champa incense sticks.
Label information: Nag Champa Agarbatti Satya Sai Baba. Mfrs. Shrinivas
Sugandhalaya(BNG)LLP.1/9,8th Cross, Magadi Road, Bengaluru-560023, India. Certified green
product. Export Quality.2021 Series. Hand Rolled in India. UPC 8904245400491.Warning: insist for this label to avoid imitation buy from reputed dealers only. Earth. Contains seals with hologram over each side of the box with official logo. NetWt.40g. Quality assurance labels are not actual stickers demonstrating actual checks, but are instead printed onto the package to appear as if they were actual quality assurance stickers and are offset with a white background to trick a consumer. There are three which areas follows. Fake QA sticker1: Quality Assurance Management ISO 9001(check mark symbol)
Fake QA sticker2: Environmental Management ISO 14001(check mark symbol) Fake QA sticker 3: Occupational Health &
Safety OHSAS 45001 (check mark symbol).
Customer care number+917022000111
Item purchased at Archimage. Not their fault. They only buy reputable authentic items and this has to be a bad or contaminated batch here. | Symptoms: Nausea, Other See Less
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I shipped Priority Express on Nov 15 to Essex Junction, VT and after two days it is still showing arrived at Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA on 11/15/2021 at 9:22pm. It should be delivered by Nov 16 at VT See Less
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Teterboro, NJ USPS, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
2 weeks ago
Package was supposed to be delivered November 6, 2021.
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Odor-Eaters®, owned by Blistex Inc., is voluntarily recalling a total of forty-one lots of two Odor-Eaters® spray products to the consumer level due to the presence of benzene. Internal testing identified low levels of benzene contamination in specific lots of these aerosol products.
Risk Statement: Benzene is... See More classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening.
To date, Odor-Eaters® has not received any reports of adverse events related to this recall. The affected Odor-Eaters® spray products are used as antifungal and foot odor-reducing agents and are packaged in aerosol cans. See the link below for UPC, lot number and expiration dates. Refer to the image below for guidance on where to find the lot code details on the can. Forty-one lots of two Odor-Eaters® spray products (Odor-Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray) are impacted by this voluntary recall, specifically the ones listed in the link below.
The products were distributed nationwide in the United States through various retailers. Consumers, distributors, and retailers that have product which is being recalled should stop using or selling these specific Odor-Eaters® spray products and dispose of them appropriately.
Company name: Odor-Eaters®, owned by Blistex Inc.
Brand name: Odor-Eaters®
Product recalled: Oder Eaters spray products
Reason of the recall: Due to the presence of benzene
FDA Recall date: November 17, 2021
Check the full recall details on fda.gov
Source: FDA See Less
101
DreamBone Twist Sticks are making my dogs vomiT - from Chewy.com., Hickory Valley, TN, USA
2 weeks ago
DreamBone Twist Sticks are making my dogs vomit. They were purchased from Chewy.com.
I have been giving our dogs Dream Sticks with no problem. Three of our dogs started vomiting this morning and two have continued vomiting throughout the day. Our Pyrenees-Lab has vomited six times so... See More far today and STILL pieces of DreamBone Twist Sticks See Less
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Sagent Pharmaceuticals, Inc. on November 19 announced the voluntary nationwide recall of four lots of Levetiracetam Injection, USP, to the user level. The lack of container closure integrity, found in reserve sample vials may result in a non-sterile product.
Risk Statement: Intravenous administration of a product intended... See More to be sterile that is not sterile could result in serious systemic infections which may be life-threatening.
To date, Sagent has not received reports of any product complaints or adverse events associated with this issue. Levetiracetam Injection, USP 500 mg per 5 mL, is used in the treatment of certain types of seizures and is packaged in a 5mL single-does vial. The Levetiracetam Injection, USP, label and affected lot numbers with Expiration Dates and NDC number can be found in the table below.
Product: Levetiracetam Injection, USP / Lot Number: B0G85VB /Expiration Date: Jun-2022 / NDC Number: 25021-780-05 / Distribution Dates: May 2021 - August 2021.
Product: Levetiracetam Injection, USP / Lot Number: B0K88VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: March 2021 - November 2021.
Product: Levetiracetam Injection, USP / Lot Number: B0K89VA /Expiration Date: Sep-2022 / NDC Number: 25021-780-05 / Distribution Dates: August 2021 - November 2021.
Product: Levetiracetam Injection, USP / Lot Number: B1G194A /Expiration Date: Jun-2023 / NDC Number: 25021-780-05 / Distribution Dates: October 2021.
The product was distributed Nationwide from March to November 2021.
Company name: Sagent Pharmaceuticals, Inc.
Brand name: Sagent
Product recalled: Levetiracetam Injection
Reason of the recall: Lack of sterility assurance
FDA Recall date: November 22, 2021
Check the full recall details on fda.gov
Source: FDA See Less
101
Mountain Meadow Herbs of Somers, MT is recalling 54 bottles (total 240 capsules per bottle) of Mountain Meadow Herbs brand Candida Flush, Lot# 0120011Q. Some bottles from this Lot have become pressurized over time in storage. When opened, the product may forcefully expel air as well as... See More portions of capsules and powder. This may result in customers sustaining injuries to their hands and eyes, which may require medical attention.
Product was distributed to retailers in IN, MN, MT, NY, TN and in Ontario of Canada.
Product was sold directly to consumers in IN, KY, MN, MO, MT, NE, OH, PA, VA, and WI. The affected Candida Flush has the UPC 8 13086 01593 2, Lot #012001l Q, Exp 12/22.
No illnesses or serious injuries have been reported to date. The recall was the result of an internal investigation stemming from a customer complaint which revealed that the finished products were becoming pressurized over time.
This recall is being made with the knowledge of the U.S. Food and Drug Administration. If you have any of these products, please dispose of them immediately.
Company name: Mountain Meadow Herbs
Brand name: Mountain Meadow Herbs
Product recalled: Candida Flush
Reason of the recall: Due to exploding bottle risk
FDA Recall date: November 17, 2021
Check the full recall details on fda.gov
Source: FDA See Less
2
Nutrisure Ltd is recalling Naturya Hemp Protein Powder because it contains gluten, which is not mentioned on the label. This means the product is a possible health risk for anyone with an allergy or intolerance to gluten. This batch was only sold in Sainsbury’s stores.
Naturya Hemp... See More Protein Powder (100g)
Pack size: 100g
Batch code: W02135
Best before: end of March 2024
Allergens: Gluten
If you have bought the above product and have an allergy or intolerance to gluten, do not eat it. Instead, return it to the store from where it was bought for a full refund.
Company name: Nutrisure Ltd
Product recalled: Naturya Hemp Protein Powder
FSA Recall date: 11/30/2021
Check the full recall details on food.gov.uk
Source: FSA See Less
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