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Recent Interesting Reports
Blackcass.com, Chain & saw are a scam!, Forsyth, MO, USA
Forsyth, MO, USA
February 13, 2021 3:46 PM
“I bit and bought a $30 GT A26 saw and found out after I had ordered it, that it was only a chain. I contacted the company and said I wanted to upgrade to the $60 chainsaw that was on their website and they said no problem & I would get the whole thing. I just received it and it is a completely diff... See Moreerent chainsaw and now the saw is not on their website anymore. Wondering how I can get my money back. See Less”
Helpful
1 person found this review helpful
Covid 19 vaccine symptoms, Indianapolis, IN, USA
Symptoms: Nausea
Headache
Fatigue
Skin Rash
Soreness
Indianapolis, IN, USA
February 2, 2021 10:30 PM
“I am a female, 26 years old.An RN at Riley Children’s hospital. I received the moderne vaccine. The first dose, the physical shot was less painful than flu vaccine. Only symptom was sore arm for 2 days. Second dose, much worse. Woke up 24 hrs later feeling fatigued, nauseous, headache, and developed... See Morelarge red circular rash around injection site. Lasted 24 hours. Was hot to touch and very painful. No fevers. Better the next day. See Less”
Helpful
4 people found this review helpful
February 3, 2021 1:00 PM
“Company name: Apotex Corp
Brand name: Apotex Corp.
Product recalled: Enoxaparin Sodium Injection, USP
Reason of the recall: Packaging error resulting in incorrect dosage listed
FDA Recall date: February 03, 2021
Recall details: Apotex Corp is voluntarily recalling two (2) batches of Enoxaparin... See MoreSodium Injection, USP to consumer level due to a packaging error resulting in some syringes barrels containing 150 mg/mL markings (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL markings (corresponding to 100 mg/mL strength) on the syringe barrel and vice versa. The packaging error was discovered during a customer complaint investigation. To date, Apotex has not received any reports of adverse events related to use of these two batches. The affected product is manufactured by Gland Pharma Limited, Hyderabad, India.
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
Source: FDA See Less”
Helpful

Pfizer Covid 19 vaccine, Alamodome, Montana Street, San Antonio, TX, USA
Alamodome, Montana Street, San Antonio, TX, USA
February 5, 2021 8:50 PM
“I received my first vaccine at Alamodome on January 20 and will get second vaccine February 10. The Alamodome was very organized and the people who worked there very professional. I had no reactions to first shot which was Pfizer See Less”
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1 person found this review helpful
Scam by Blackcass of Houston, TX or LA, CA or probably China somewhere., South Jordan, UT, USA
South Jordan, UT, USA
February 17, 2021 6:09 PM
“A scam regarding a small knock-off chain saw that is the center of a scam by Blackcass of Houston, TX or LA, CA or probably China somewhere. We ordered a Blackcass 2020 Hot selling GTA 26 Battery-Powered Wood Cutter X 1 in December 2020. We did received, via USPS, a 25" long segment of chain saw l... See Moreinks with Orange handles on each end, so it is NOT Battery-Operated. One of the photos in the Blackcass ad that are associated with this SCAM are EXACTLY the same photo used by the very legitimate Stihl company model GTA-26...only the word, "Stihl" is omitted on the Blackcass ad's photo. So, consumers and the real manufacturer are BOTH being scammed. See Less”
Helpful
Pfizer Vaccine side effects, Pittsburgh, PA, USA
Symptoms: Headache
Soreness
Skin Rash
Pittsburgh, PA, USA
February 1, 2021 4:52 PM
“Morning recieved: Arm sore. Headache. Then broke out in welt type hives from my face down to my toes. Had to go to ER for epi pen and steroids. See Less”
Doctor Visit: Yes
Diagnosis: ER
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February 7, 2021 11:58 PM
“The FDA observed the website offers “Corona Destroyer Tea” for sale in the United States in two options, “Prevention” and “Reversal,” and that this product is intended to mitigate, prevent, treat, diagnose, or cure COVID-19[1] in people.
Based on FDA review, this product is an unapproved new dr... See Moreug sold in violation of section 505(a) of the Federal Food, Drug, and Cosmetic Act (FD&C Act), 21 U.S.C. § 355(a). Furthermore, this product is a misbranded drug under section 502 of the FD&C Act, 21 U.S.C. § 352. The introduction or delivery for introduction of this product into interstate commerce is prohibited under sections 301(a) and (d) of the FD&C Act, 21 U.S.C. § 331(a) and d. Some claims on the website and product label establish the intended use of the product and misleadingly represent it as safe and/or effective for the treatment or prevention of COVID-19
For more information click here: fda.gov See Less”
Helpful
2 people found this review helpful
Second Moderna vaccine shot, New York, NY, USA
New York, NY, USA
February 11, 2021 5:22 PM
“Got my second Moderna Covid-19 vaccine shot, no side effects this time. A little tired and thirsty but so far so good. See Less”
Helpful
1 person found this review helpful
February 10, 2021 10:00 PM
“Company name: NDAL MFG INC
Brand name: ManukaGuard
Product recalled: Allercleanse Nasal Spray
Reason of the recall: Due to Yeast Contamination
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.
Risk Statement: The use of Allercleanse (manuka honey) nasal spray contaminated with yeasts, in the population most likely to use it (children, adults, and elderly), may result in adverse events that necessitate medical or surgical intervention. However, use of this contaminated product in immunosuppressed individuals may result in life threatening invasive fungal infections.
NDAL MFG INC has not received any reports of adverse events related to this recall. The product is used as a NASAL SPRAY to clean nasal passages and sinuses of irritants and other environmental contaminants and is packaged in cardboard box with one nasal spray per box UPC 858631002128. The affected Allercleanse lot is lot # 2010045 and BB 10/2023 expiration date.
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.
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
Blackcass.com, Fraud, Flagler Beach, Florida, USA
Flagler Beach, Florida, USA
February 4, 2021 9:46 AM
“I ordered a hand chainsaw and only received the chain after waiting over a month. Website said it was coming from California but it came from China. They will not give me a refund. See Less”
Helpful
1 person found this review helpful