Source: env.nm.gov
1079 New Mexico Avenue, Holloman Air Force Base, New Mexico, United States
Updated:
Source: env.nm.gov
Recent Interesting Reports
Alert of a cluster of Illnesses resembling Botulism from possibly Counterfeit Botox, LaSalle County, IL, USA
2 weeks ago •source dph.illinois.gov
Outbreak
The product in question is either Botox or a possibly counterfeit version of the product, and it was administered by a licensed nurse in LaSalle County who was performing work outside her authority. The two affected individuals reported symptoms such as blurred/double vision, droopy face, fatigue, shortness of breath, difficulty breathing, and hoarse voice following the injection. Both required hospitalization post-treatment.
People are advised not to use these botox injections. In Illinois, the injection of botulinum toxin, the key ingredient in Botox, is a practice of medicine that may only be performed by certain licensed professionals who are licensed and regulated by IDFPR. Cosmetologists and estheticians are prohibited from performing this practice under their licenses.
Botulism is a serious illness caused by a toxin produced by the Clostridium botulinum bacteria. This toxin is one of the most potent neurotoxins known and can cause muscle paralysis. The disease can manifest in three forms: foodborne botulism, wound botulism, and infant botulism. Foodborne botulism, which is the focus here, occurs when food contaminated with the bacteria is consumed. Symptoms can include difficulty swallowing or speaking, facial weakness, and paralysis. In severe cases, it can be fatal, particularly if it affects the respiratory muscles.
If you or a loved one are harmed or experiencing any symptoms, it is important to report it. Reporting can help to detect & resolve outbreaks early and prevent others from being harmed, and enables better surveillance. If symptoms persist, seek medical care.
Source: dph.illinois.gov
DGTGOODSGONS, Barletta, Province of Barletta-Andria-Trani, Italy
1 week ago •reported by user-hgfc4487
Received daily detox did not order, Jamestown, TN, USA
1 week ago •reported by user-qwdky314
Unordered Package, Bridgeport, CT, USA
1 day ago •reported by user-yrhww433
Order, Everett, Massachusetts, EE. UU.
3 weeks ago •reported by user-xzfq7797
Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA
2 weeks ago •source www.fda.gov
Recall notice
The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651
Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.
Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.
Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024
Source: www.fda.gov
VERTI bioribose that was’t ordered, don’t need and don’t want., Dallas, GA, USA
5 days ago •reported by user-whpg7377
I am reporting a scam, Alabama, USA
3 weeks ago •reported by user-cxtv4755
Keep sending product. Want to cancel., Wichita, KS, USA
1 week ago •reported by user-xytn2795
Unordered package from Rosewood P, Renton, WA, USA
2 weeks ago •reported by user-dtyy3926
Report by
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