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Dunkin', 876 Edgell Rd, Framingham, MA 01701, USA
Total all time reports:
1
Latest report: May 28, 2020 12:00 PM
More incidents from:
Bakery
Cafe
Meal takeaway
Restaurant
Coronavirus - Covid-19
Dunkin donuts
876, Edgell Road
Framingham
Massachusetts
United States
Dunkin' Employee Test Positive For COVID -19
May 28, 2020 12:00 PM
“An employee at the Dunkin’ on Edgell Road has tested positive for COVID-19. the employee last worked on May 25. If you visited the restaurant during that time, please report it and any other location that you visited.
Source: framinghamsource.com See Less”
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2 people found this review helpful
LONG TERM continued extreme immune response to Pfizer vaccine, Danville, PA, USA
Symptoms: Fever
Other
Chills
Chest Pain
Swelling
Danville, PA, USA
May 12, 2021 5:59 PM
“I am going to post my entire diary. Those who truly want to know won't mind reading the entire thing and...it's still not over yet.
Pfizer 51 day systemic reaction
(now beyond day 77)
Danville, PA
*Not a complaint*
(wasn't at the time)
I had left prior short term reviews on both do... See Moreses, now I am finally able to detail my entire reaction which was shocking to me honestly. Arthritis/fibro/immune compromised patients be advised.
After dose 1 on 3 Mar, it simply made my left hand ballooned then arthritic (never had arthritic hands before this) and it seemed as if it was going to relent, but kept coming and going, then eventually this spread to both hands and ankles. I gained 3 pounds of water weight. The pain was maddening from day 8 on, coming and going.
Day 12 I had routine nonsteroidal spinal injections. MISTAKE. I wouldn't advise doing this but it was urgent as I needed the injections to have the capability to drive to dose 2. My whole left side's injection sites swelled and scabbed over several days. (never had that happen in 12 years of receiving them) I could not sit down, lie down, or touch the sites but it resolved quickly in my opinion. The hand pain stayed the course until...
Dose 2 I was thankful to receive and looked forward to my newfound freedom. 1 Apr I had the minor eye floaters on the way home just like dose 1. I felt like a dead dog so fell asleep on the couch as soon as I walked through the door. 7 hours later developed chills and mild fever and leg (quads) pain. No big deal I thought as this happens to everyone. I began consuming electrolytes and rode the fever out with the aid of Ibuprofen. My last review ended with me saying I expect a 1 to 2 day recovery. That is not what really happened.
Following dose 2 ( lot # EP7534) I suffered an entire body inflammatory response.
The leg pain became so severe I had difficulty walking or doing anything at all for 8 days. Any attempt at physical activity doubled the pain. This is when I had my first Dr appointment and I was told to be patient and it should resolve in 2 to 4 WEEKS, and if not I need to be tested for Rheumatoid. I waited patiently and prayed for this to end. As a former athlete, I will admit to being way less sore after running a marathon.
The legs began to ease up but it traveled back to my hands, then to my lower back, then to my knees and feet. Called our Covid hotline at least 4 times during the 3 week course of this barrage and was told that this kind of reaction is almost unheard of. It then hit my hips. This was so excruciating for a week I had to lift my legs by hand to get up, and once again I could walk but didn't desire to. Next doctor appointment, was advised if the pain will not resolve in a timely manner, I need a full examination and bloodwork for gout and 7 other tests were ordered.
While laid up, incidentally my Father received dose 1 of Moderna. He was symptom free until Day 8, then, had the exact same reaction but on a lesser scale. It was then I started to believe something in our genetics is causing it. Day 52, it FINALLY began subsiding. The swelling reduced and became localized to the right knee (prior injury) and the left hand.
Overall, this was a severe reaction but I do not solely blame the vaccine. I am a 43 year old woman with Fibromyalgia and a slew of other compromising health issues. These companies did their ultimate best to save lives, perhaps mine included. Although devastated to seemingly have permanent damage to the knuckles of my left hand, tissue of the right knee and knuckles of my foot, there has been far greater devastation from Covid, including losing a family member.
I am extremely hesitant towards the booster, but I need the protection to feel at peace with sending my children back to school. I will follow my doctor's advice and the Covid team's direction to fill out the VAERS surveys for both doses. This information is found in small print on the back of the card.
*CONTINUED*
It did NOT end here either. 48 hours after the joint pain "subsided," I went to bed thinking it was all over then woke up in Tachycardia shortly after midnight with a heart rate of 156! ? For 3 days I had my daughter sleep in my bed with me as I battled a severely irregular heart beat. This was preposterous as I spent decades as a personal trainer and thought (knew!) I had a very healthy heart?
On the 3rd day of being stuck in chronic tachycardia episodes, my daughters ended up urgently calling family and an ambulance because I felt symptoms of a possible stroke.
In the ambulance my BP had escalated to 167/110 and normal for me is actually always quite low. In fact I had a reading of 117/74 the week prior during an unrelated visit. I have never had a high blood pressure reading in my entire life not from any illness or activity ever!
At the hospital I was informed my kidneys had astonishingly dropped to less than 40% of function and I was in real trouble. They stabilized me and sent me home, then a day later I went right back into tachycardia for an additional 3 days. I did the equivalent of a marathon or more each night IN MY SLEEP. I was given a heart monitor to record the activity and set up with an urgent echocardiogram and CT of my heart. With a blood clotting disorder, I could not afford to mess around any longer and had to leave my kids once again to be driven to the ER. 7 additional hours I spent with a pulse often above 150. I was finally given a Beta blocker and also an antibiotic, as the dehydration this was causing me erupted into a kidney infection which was throbbing on my right side.
I feared for me life. I feared for my vitality as my Pain treatments were stripped away due to the suspected heart condition. All my heart tests came back completely normal and I was told my heart is oddly not the source of my heart condition. A relief yes, but just further proof of how extremely and completely this vaccine attacked my body.
I was having chest pains the week prior and the week of these attacks which was finally concluded to be new Costochondritis, a rare flareup which can happen with Fibromyalgia. Thank God that's all it is but I am so through with this vaccine now and the utter devastation it has caused my entire body. I am having trouble breathing and the umpteen hospital visits have ruled out everything else. It is not anxiety but I will admit alas I have begun to grow impatient with this!! I have 1/2 dozen medical professionals in contact with me daily now working on a way to get me to the finish line.
After clearing my heart tests, I was reinstated for Pain Management and was brought in immediately for an appointment. My back underwent approximately 30 trigger point injections and there was not a location on my body without a muscle spasm. My last injections were rejected by my body due to the presence of the vaccine and I prayed this time they wouldn't be. During the procedure I suffered an immediate inflammatory response, elevated blood pressure, etc etc. My skin reacted so badly my administrator could not even apply the bandages. 13 years getting these injections and no problems until right now!
Next day it started happening all over again. My body (more specifically, the vaccine within my body) began to reject some of my treatment in the lower region. I am now being put on a steroid to combat the vaccine and widespread pain reaction of the chest, legs, hips, extremities, and back. I continue to take the Beta blocker now as well.
10 weeks of suffering I just want it to end but more importantly I have to stay vigilant in getting my story told. I'm willing to bet a reaction like this will turn out not to be so rare. In fact my Father is still laid up just the same as me he's in week 5 battling Moderna and also on a long road. My final report to the CDC will be submitted after further bloodwork, but it is to be made absolutely clear that if I have now developed an auto-immune condition...the vaccine triggered it.
Good luck to everyone but honestly weigh the decision heavily before you enter the unknown. See Less”
Doctor Visit: Yes
Diagnosis: ER
Helpful
21 people found this review helpful
May 11, 2021 3:01 PM
“Company name: Dash Xclusive
Brand name: Imperia Elita
Product recalled: Vitaccino Coffee weight loss and anxiety dietary supplement
Reason of the recall: Undeclared Sibutramine and Fluoxetine
FDA Recall date: May 11, 2021
Recall details: Glendale, California, Dash Xclusive is voluntarily recal... See Moreling all lots of Imperia Elita Vitaccino Coffee to the consumer level. FDA analysis has found the product to contain undeclared sibutramine and fluoxetine. Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues, including stroke, heart failure and serious health risk especially to those with underlying heart related disease.
Fluoxetine is an FDA approved drug indicated for the treatment of various depressive disorders, obsessive compulsive disorder, bulimia and panic disorders. This drug product carries a box warning for suicidal thoughts and behaviors and it needs to be monitored closely by a prescriber. The presence of sibutramine and fluoxetine in Imperia Elita Vitaccino coffee renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. Dash Xclusive has not received any reports of adverse events related to this recall.
Risk Statement: Products containing undeclared sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. Products containing undeclared fluoxetine could cause suicidal thinking and behavior, an accumulation of high levels of serotonin in the body or neuroleptic malignant syndrome (NMS)-like reactions which is a life-threatening neurological disorder; elevated mood state that can cause higher than normal energy levels, restlessness, decreased need for sleep; abnormal bleeding, and low sodium levels.
The product is marketed as a dietary supplement for weight loss and is packaged in a black rectangular box and contains fifteen sachets. The affected Imperia Elita Vitaccino coffee lots include all lots. Product was distributed Nationwide in the USA via internet and by ebay at www.ebay.com. On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.
Dash Xclusive is notifying its customers by e-messages on the eBay platform and is arranging for return of all recalled products. Consumers that have Imperia Elita Vitaccino Coffee which is being recalled should stop using/return to Dash Xclusive, 610 S. Verdugo Road, Apt 31, Glendale, California 91205. Consumers with questions regarding this recall can contact Dash Xclusive by e-mail at dashxclusive11@gmail.com on Mondays to Thursdays from 11am to 4pm Pacific Time zone.
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. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online by regular mail or by fax. Complete and submit the report Online. Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
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April 30, 2021 6:01 PM
“Company name: Acella Pharmaceuticals, LLC
Brand name: Acella
Product recalled: NP Thyroid (Thyroid Tablets, USP)
Reason of the recall: Sub potency
FDA Recall date: April 30, 2021
Recall details: Acella Pharmaceuticals, LLC, is voluntarily recalling certain lots listed in the Tables 1 and 2 belo... See Morew of 15-mg, 30-mg, 60-mg, 90-mg and 120-mg NP Thyroid®, Thyroid Tablets, USP [levothyroxine (T4) and liothyronine (T3)] to the consumer level. The products are being recalled because routine testing has found these lots to be sub potent. The product contains less than 90% of the labeled amount of liothyronine (T3) and/or levothyroxine (T4).
Risk Statement: Patients being treated for hypothyroidism (underactive thyroid), who receive sub potent NP Thyroid®, may experience signs and symptoms of hypothyroidism (underactive thyroid) which may include, fatigue, increased sensitivity to cold, constipation, dry skin, puffy face, hair loss, slow heart rate, depression, swelling of the thyroid gland and/or unexplained weight gain or difficulty losing weight.
There is reasonable risk of serious injury in newborn infants or pregnant women with hypothyroidism including early miscarriage, fetal hyperthyroidism, and/or impairments to fetal neural and skeletal development. In elderly patients and patients with underlying cardiac disease toxic cardiac manifestations of hyperthyroidism may occur, such as cardiac pain, palpitations, or cardiac arrhythmia.
To date, Acella has received 43 reports of serious adverse events that could possibly be related to this recall. NP Thyroid®, Thyroid Tablets, USP is composed of levothyroxine and liothyronine, and used to treat hypothyroidism (underactive thyroid). The products subject to recall are packed in 100-count and 7-count bottles. See product images below. To best identify the product, the NDC’s, Product Description, Lot Numbers, and Expiration Dates are listed on the link below.
These lots were distributed nationwide in the United States to Acella’s direct accounts, including wholesalers, pharmacies, and healthcare offices. Acella is proactively notifying its consignees to discontinue distribution of the above referenced lots being recalled and is arranging for return of all recalled products. Patients who are currently taking NP Thyroid® from the lots being recalled should not discontinue use without contacting their healthcare provider for further guidance and/or a replacement prescription.
Consumers with questions about the recall can email Acella Pharmaceuticals at recall@acellapharma.com or contact our representatives at 1-888-424-4341, Monday through Friday from 8:00 am – 5:00 pm ET. 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. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
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Headache
Dizziness
Fatigue
Body Ache
Soreness
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I have not received the product, Fort Myers, FL, USA
Fort Myers, FL, USA
May 10, 2021 1:47 PM
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Transaction # 1ym4274N33939154. I really need them as they were gifts. One of them was my husband's birthday present at the end of March They were ordered early and they removed t... See Morehe money from my account March 6, 2021. They still show them on FB. They also sent that email to me. After checking with others, information is not correct. Never delivered. See Less”
Helpful
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Chainsaw scam, Bethlehem, PA, USA
Bethlehem, PA, USA
May 2, 2021 11:28 PM
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A Scam by Blackcass.com, Redwood City, CA, USA
Redwood City, CA, USA
April 21, 2021 12:38 PM
“Blackcass.com is a total scam. My wife bought me what she thought was a mini electric chain saw. The site showed a sthil chain saw for $29.99 instead of $59.99. Not knowing the prices on tools she thought to surprise me. The next day I found her order in our computer and immediately contacted them a... See Morend tried to cancel it. They said it was too late as the order had already been processed. 10 weeks later we got a hand rose clipper instead. My wife had paid $37.99 for a clipper I got at Ace hardware before for $9.99 See Less”
Helpful
1 person found this review helpful
May 13, 2021 3:03 PM
“Company name: Scentsational Soaps & Candles, Inc.
Brand name: Goose Creek, COCO TKO
Product recalled: Hand Sanitizer
Reason of the recall: Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde
FDA Recall date: May 13, 2021
Recall details: Scentsational Soaps & Candles, Inc., has volunta... See Morerily expanded its April 27 recall of scented Hand Sanitizers to include three lots of Goose Creek HAND SANITIZER (NDC 75078-004) + Aloe and one lot of COCO TKO HAND SANITIZER in 3.38 and 3.4 fluid ounce spray bottles, respectively, to the consumer level.
These products are listed in the table below. These products are being recalled after testing conducted by our firm revealed the presence of methanol (wood alcohol), benzene, and acetaldehyde. These products were sold on the Internet and distributed nationwide in the USA by Goose Creek Candles, LLC and Coconut Stand.
- Goose Creek HAND SANITZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Blueberry Limeade Anti-Bacterial Spray. UPC or NDC: NO UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe (3.38 fl oz. (100 ml)). Scent: Limoncello Anti-Bacterial Spray. UPC or NDC: NO UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Beach Dreams Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Grape Soda Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Champagne Bubbles Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Dragonfruit Splash Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Marshmallows Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Melon Picnic Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 35 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Optimistic Vibes Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Red White and Blue Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 42 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Watermelon Lemonade Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 35 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Tropical Daydream Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20260. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- COCO TKO HAND SANITIZER (3.4 fl oz. (100.55 ml)). Scent: Coconut Stand. UPC or NDC: No UPC. Lot: 20260. Retailer and States shipped: 14 cases shipped on 9/16/20 to FL.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning. Exposure to benzene can occur through inhalation, oral, and skin.
There is a reasonable probability that benzene present at levels above the maximum daily exposure recommendations can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Additionally, animal studies have shown that acetaldehyde can possibly cause cancer in humans. To date, the company has not received any reports of adverse reactions related to this recall.
These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The affected bottles of hand sanitizer include a five-digit lot code printed on the bottle near the base. The products can be identified by the label, scent, and lot code provided in the table at the end of this release. Photos are also provided at www.scentsational-products.com.
Scentsational Soaps & Candles, Inc. has notified its direct customers by telephone with confirmatory email and asked that they remove the recalled products from commerce immediately if they still had any in inventory. Consumers, distributors, and retailers that have the hand sanitizers which are being recalled should stop using, distributing and/or selling them and return them to the place of purchase.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA See Less”
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Pfizer BioNTech vaccine, Walgreens, Ohio 43, Streetsboro, OH, USA
Symptoms: Fatigue
Lightheaded
Muscle Pain
Soreness
Walgreens, Ohio 43, Streetsboro, OH, USA
April 28, 2021 5:52 PM
“Got the first dose of the Pfizer vaccine yesterday at Walgreens. Process was very smooth, no allergic reactions. Had some initial wooziness and lightheadedness 5 minutes after receiving the vaccine but may have just been anxiety.
Symptoms after 27 hours: sore arm, joint and muscle pain, fatigue.... See MoreFeeling warm/flushed but no fever. See Less”
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