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Covid-19 OSHA Complaint, Macerich Management Co, 293 Valley River Ctr, EUGENE, OR, 97401, USA

February 10, 2021 12:00 PM

293 Valley River Center, Eugene, 97401 Oregon, United States

Serious

Alleged Hazards: 1,
Source: Osha.gov | Receipt Date: 2020-11-16

Reported By SafelyHQ.com User

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Recent Interesting Reports

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
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January 27, 2021 9:01 PM

“Company name: Meitheal Pharmaceuticals, Inc.
Brand name: Meitheal Pharmaceuticals, Inc.
Product recalled: Cisatracurium Besylate Injection, USP 10mg per 5mL
Reason of the recall: Mislabeling
FDA Recall date: January 27, 2021
Recall details: Meitheal Pharmaceuticals, Inc. (“Meitheal”), annou... See Morenced today that it is voluntarily recalling one (1) lot of Cisatracurium Besylate Injection, USP 10mg per 5mL to the user level. The decision to recall the product was made after a product complaint revealed that a portion of Lot C11507A of cartons labeled as Cisatracurium Besylate Injection, USP 10mg per 5mL, containing 10-vials per carton, contained 10-vials mis-labeled as Phenylephrine Hydrochloride Injection, USP 100mg per 10mL. 

To date, Meitheal has not received reports of any adverse events or identifiable safety concerns attributed to the lot. There is a reasonable probability that a patient who requires cisatracurium for muscle paralysis as part of general anesthesia is administered phenylephrine instead would not receive any skeletal muscle relaxation and could cause a hyperadrenergic state resolution in elevated blood pressure, arrhythmia and cardiac/brain ischemia.  If this is not quickly diagnosed and treated, severe illness or death can occur. 

There is a reasonable probability that a patient who requires phenylephrine to increase their blood pressure, such as patients with severely low blood pressure, especially resulting from septic shock who is administered cisatracurium instead could result in a fast onset of muscle paralysis and decrease in oxygen. If this is not quickly diagnosed and treated, severe illness or death can occur within minutes. Cisatracurium Besylate Injection is used as a nondepolarizing neuromuscular blocker. 

The affected Cisatracurium Besylate Injection lot being recalled is C11507A, EXP. October 2021.  The product can be identified as a 5mL vial stoppered with a rubber stopper and sealed with aluminum seal having an Aqua color flip-off seal.  Meitheal commenced shipping the product to customers on August 19, 2020 which was distributed to wholesalers nationwide in the USA.

- Cisatracurium Besylate Injection, USP 10mg per 5mL. Lot Number: C11507A*. Expiration Date: October 2021*. NDC Number: 71288-712-06 (unit of sale) |71288-712-05 (unit of use). Distribution Dates: August 19, 2020 – January 04, 2021.

*Note: Mis-labeled product will have this same Lot Number of C11507A and Expiration Date of October 2021 but will be labeled on the vial as Phenylephrine Hydrochloride Injection, USP 100mg per 10mL, NDC 71288-808-77 (unit of use).

Meitheal has notified its distributors and customers in writing to arrange for return of all recalled product. Customers who have purchased the product should not open the carton or use its contents and should immediately quarantine and return the recalled lot of product. Customers who may have further distributed this product should promptly identify their customers and notify them at once of this product recall.

Consumers with questions regarding this recall can contact Meitheal’s Customer Service weekdays 8:00AM to 6:00PM CST at 844-824-8426. 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, as follows.

Check the full recall details on fda.gov

Source: FDA
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February 10, 2021 10:00 PM

“Company name: NDAL MFG INC
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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
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Door frames, bed frame, cabinets and air vents, Philadelphia, PA, USA

Symptoms: Other Dehydration Headache Muscle Pain
Philadelphia, PA, USA

February 2, 2021 9:31 PM

“I am sick., My apartment has a rusting metal. Continuous everyday. I have reported to Cyber Village management and staff that there is a substance causing the metal to rust in my apartment. It is a colorless and odorless substance that rusts metal. This poisonous substance is in my food, clothes,... See Morehair shampoos and conditioners, hand and body lotions and all over my apartment. This poisonous substance is making me sick. This substance causes a dehydration. Also, this poison causes metal to RUST. The evidence of this Rust is on the following: Bathroom door frame and all metal objects in the bathroom are RUSTED Recliner is RUSTED Bedframe is RUSTED Air Vents rusted It is colorless and odorless; however, the effects are server chest congestion, cough, eye and throat irritation. It dries the air which dries my body and my nasal area. It causes server headache and chest/head congestion. It also causes muscle pain and darkens my skin. Also, I have the feelings of pins and needles on hands and feet when it is present on my furniture. I belive someone is poisoning me. This is dangerous for me as well as the community. If this is done to me, it can happen to anyone. See Less
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February 23, 2021 1:16 PM

“I ordered the Mini chain saw and the picture on the right is what i got. What the hell am i supposed to do with a chain without the saw. I am on social security and can not afford to give idiots my money. Some bastard out there is getting rich off trusting people. I want my d**n money back or i get... See Morea lawyer. I hate a f*****g thief! See Less
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January 28, 2021 7:00 PM

“Company name: Wahl Clipper Corporation
Brand name: Wahl
Product recalled: Deluxe Heat Therapy Massagers, Model 4212
Reason of the recall: Can overheat causing smoke or spark, which may pose a fire hazard
FDA Recall date: January 28, 2021
Recall details: Wahl Clipper Corporation is voluntarily... See Morerecalling all Deluxe Heat Therapy Massagers, Model 4212. Discontinue use immediately. The connection between the massager and heat attachment can overheat causing smoke or spark, which may pose a fire hazard. The image below shows the area where smoke or sparks may appear.

If you own a Deluxe Heat Therapy Massager, call us at 800-767-9245 or email at techsupport@wahlclipper.com. We will facilitate the free return of your unit in exchange for a full refund plus an additional $10 for this inconvenience. Your safety is important to Wahl Clipper Corporation. If you have any questions concerning this voluntary product recall, please contact us.

Check the full recall details on fda.gov

Source: FDA
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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
Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: ER

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
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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
Reported By SafelyHQ.com User

January 29, 2021 10:47 AM

“Alternative Foods London Ltd is recalling OGGS Zesty Lemon Cake because it contains soya that is not declared on the label. This means the product is a possible health risk for anyone with an allergy to soya.

Product details
OGGS Zesty Lemon Cake
Pack size 386g
Best before 26 January 2021; 02... See MoreFebruary 2021; 09 February 2021 and 16 February 2021
Allergens Soya
Risk statement
Allergen(s): Soya

This product contains soya making the product a possible health risk for anyone with an allergy to soya.

Alternative Foods London Ltd is recalling the above product from customers and has contacted the relevant allergy support organisations, which will tell their members about the recall. The company has also issued a point-of-sale notice to its customers. These notices explain to customers why the product is being recalled and tell them what to do if they have bought the product. Please see the attached notice.

If you have bought the above product and have an allergy to soya, do not eat it. Instead return it to the store which you purchased it for a refund.

Check the full recall details on food.gov.uk

Source: FSA
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Reported By SafelyHQ.com User