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Diagnosis: Bacterial

Updated:

A
The Los Angeles County Department of Public Health cautions residents who are planning to visit certain Los Angeles County beaches to avoid swimming, surfing, and playing in ocean waters due to bacterial levels exceeding health standards when last tested.

BEACH AREAS WARNINGS:
· Malibu Lagoon at Surfrider … See More
Beach
· Topanga Canyon Beach in Malibu
· Latigo Shore Drive in Malibu
· Escondido Creek at Escondido State Beach
· Solstice Creek at Dan Blocker County Beach
· Marie Canyon Storm Drain at Puerco Beach
· Las Flores Creek at Las Flores State Beach
· Pena Creek at Las Tunas County Beach
· Santa Monica Canyon Creek at Will Rogers State beach
· Santa Monica Pier in Santa Monica
· Pico-Kenter storm drain at Santa Monica Beach.
· Mothers Beach in Marina Del Rey

Source: www.publichealth.lacounty.gov
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#water #california #us #bacterial

Xiamen, Fujian, GFA Production (Xiamen) Co., Ltd. is voluntarily recalling one lot of Easy Care first aid® AfterBurn ® Cream, 0.9 g single-use packets. The single use packets are sold in boxes of 10 or packaged in certain First Aid kits. This recall is to the consumer … See More
level. FDA analysis found the product to be contaminated with Bacillus licheniformis, and Bacillus sonorensis. The product was distributed nationwide to retailers from March 4, 2022 through December 12, 2022. To date, GFA Production (Xiamen) Co., Ltd. has not received any reports of adverse events related to this recall.

Risk Statement: In immunocompromised patients, the topical use of the contaminated Easy Care® AfterBurn® Cream 0.9g single-use packets could potentially result in severe or life-threatening adverse events such as bacteremia, sepsis, and peritonitis. In non-immunocompromised patients, the population most likely to use the product, the use of the defective product may result in infectious complications, for instance skin infections, but in this population the infections are expected to be less severe and more readily responsive to treatment.

The Easy Care first aid® AfterBurn® Cream 0.9 g single-use packet, is used as an over the counter first-aid treatment for minor burns. The single use packets bear lot number W06I28 and are  packaged in boxes of ten or included in the certain First Aid kits named below.  

The lot number of the single use packet can be found on the back of the packet.  The lot number for the First Aid Kit that contains the single use packet can be found on each kit, either on the product hang-tag or on the bottom of the kit.

Refer to the images below for guidance on where to find the lot code details.  If your product does not have a lot code that is listed in the below table then it is not part of this recall and can be used as intended.

Package: Box of 10
Product Number: 9999-1515
Product Description: EasyCare First Aid® AfterBurn® Cream, 0.9g single-use packet
Lot number: W06I28
Expiration: 09/28/2024

Package: First Aid Kit
Product Number: 1015-0150
Product Description: Adventure® Marine 150
Lot number: W06I20
Expiration: 09/20/2024

Package: First Aid Kit
Product Number: 0120-0213
Product Description: Adventure® First Aid 1.0
Lot number: W06C05 W06F10 W06H15
Expiration: 03/05/2024 06/10/2024 08/15/2024

Package: First Aid Kit
Product Number: 0120-0212
Product Description: Adventure® First Aid 1.5
Lot number: W06H15
Expiration: 08/15/2024

Package: First Aid Kit
Product Number: 9999-2129
Product Description: Easy Care First Aid® 25 Person 2009 ANSI
Lot number: W05L28
Expiration: 12/28/2023

Package: First Aid Kit
Product Number: 9999-2128
Product Description: Easy Care First Aid® 10 Person 2009 ANSI
Lot number: W05L28 W06F10 W06H15
Expiration: 12/28/2023 06/10/2024 08/15/2021

Package: First Aid Kit
Product Number: 9999-2150
Product Description: Easy Care First Aid® Class A ANSI 25 Person
Lot number: W06C05 W06H15
Expiration: 03/05/2024 08/15/2024

Package: First Aid Kit
Product Number: 9999-2132
Product Description: Easy Care First Aid® 25 Person 2009 ANSI
Lot number: W06H15
Expiration: 08/15/2024

Package: First Aid Kit
Product Number: 2980-0700
Product Description: CVS® First Aid Home
Lot number: W06H15
Expiration: 08/15/2024

Package: First Aid Kit
Product Number: 9999-2131
Product Description: Easy Care First Aid® 10 Person 2009 ANSI
Lot number: W06H15
Expiration: 08/15/2024

Package: First Aid Kit
Product Number: 9999-2132
Product Description: Easy Care First Aid® 25 Person 2009 ANSI
Lot number: W06H15
Expiration: 08/15/2024

Retailers that have any 0.9 g single-use packets or the First Aid kit lots listed above should return them to their distributor. Consumers should stop using the Easy Care first aid® AfterBurn® Cream .9g single-use packet and discard it.

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: GFA Production
Brand name: Multiple brand names
Product recalled: After Burn® Cream and First Aid Kits containing After Burn Cream
Reason of the recall: Product is contaminated with Bacillus licheniformis and Bacillus sonorensis.
FDA Recall date: December 27, 2022

Source: www.fda.gov
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#medicaldevices #us #bacterial #cream #sourcream

Nottingham, NH, Buzzagogo Inc. is voluntarily recalling one lot of Allergy Bee Gone for Kids Nasal Swab Remedy to the consumer level due to potential microbial contamination. FDA testing found some product to contain elevated levels of yeast & mold and may contain the bacteria Bacillus cereus. … See More
Allergy Bee Gone for Kids Nasal Swab Remedy, lot # 2006491, was distributed Nationwide to wholesale distributors, retail stores and online on Amazon.com and the company web site. Buzzagogo, Inc. places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process.

Risk Statement: In immunocompromised patients, the use of the affected product could potentially result in severe or life-threatening adverse events such as bacteremia/sepsis, pneumonia, invasive fungal rhinosinusitis, or disseminated fungal infection. In non-immunocompromised patients, the population most likely to use the product, the use of the defective product may result in infectious complications, for instance bacteremia or noninvasive fungal rhinosinusitis, but in this population the infections are expected to be less severe and more readily responsive to treatment. To date, Buzzagogo, Inc. has not received any complaints related to microbial concerns or reports of adverse events related to this recalled lot.

The product is used to lessen seasonal allergy symptoms and is packaged in individual tubes for topical nasal application. The affected Allergy Bee Gone for Kids Nasal Swab Remedy lot is 2006491 with expiration date 8/2024 and UPC code 860002022116. The product can be identified by locating the lot number and expiration date on the bottom of the product carton.

Buzzagogo, Inc. is notifying its distributors and customers by email and is arranging for return or replacement of all recalled products. Consumers, distributors or retailers that have Allergy Bee Gone for Kids Nasal Swab Remedy, lot # 2006491, should stop using the product, and discard any remaining product.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.

Company name: Buzzagogo Inc.
Brand name: Allergy Bee Gone for Kids
Product recalled: Nasal Swab Remedy
Reason of the recall: Product contains elevated levels of Bacillus cereus
FDA Recall date: June 07, 2022

Source: www.fda.gov
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#drugs #recall #us #bacterial #ham

Recent Interesting Reports

Dr. Reddy's Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC: DRREDDY, along with its subsidiaries together referred to as "Dr. Reddy's"), today announced that it is voluntarily recalling six (6) lots of Sapropterin Dihydrochloride Powder for Oral Solution 100 mg to the consumer level due to … See More
powder discoloration in some packets leading to decreased potency. The issue was discovered during an accelerated stability test in addition to customer complaints. Sapropterin Dihydrochloride Powder for Oral Solution 100 mg was distributed nationwide to wholesalers/retailers. Dr. Reddy’s Laboratories Inc. has not received any reports of adverse events related to this recall to date.

Reduced efficacy of the product would result in elevated Phenylalaninemia (Phe) levels in patients. Chronically elevated Phe levels in infants and children are likely to cause permanent neurocognitive deficits, including permanent and irreversible intellectual disability, developmental delay, and seizures. Furthermore, elevated Phe levels during pregnancy, especially in early gestation, are associated with microcephaly and congenital heart disease.

The product is indicated to reduce blood phenylalanine (Phe) levels in adult and pediatric patients one month of age and older with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin-(BH4-) responsive Phenylketonuria (PKU) and is packaged in individual packets, 30 per carton. The affected Sapropterin Dihydrochloride Powder for Oral Solution 100mg lots include the following:

- Product Name: Javygtor™ (Sapropterin) Dihydrochloride) Powder for Oral Solution 100 mg, Lot Number: T2202812; T2204053; T2300975; T2300976; T2304356, Expiration date: 07/2025; 10/2025; 02/2026; 02/2026; 08/2026, NDC Number: 43598-097-30; 43598-097-30; 43598-097-30; 43598-097-30; 43598-097-30

- Product Name: Sapropterin Dihydrochloride Powder for Oral Solution 100 mg, Lot Number: T2200352, Expiration date: 12/2024, NDC Number: 43598-477-30

Dr. Reddy’s Laboratories Inc. is notifying its distributors and customers by recall notification letters and is arranging for returns of all recalled products. Anyone with an existing inventory of the product being recalled should examine the product and quarantine any of the recalled lots immediately. Consumers who have Sapropterin Dihydrochloride Powder for Oral Solution 100 mg which is being recalled should contact their physician before stopping use of the product. Consumers who have Sapropterin Dihydrochloride Powder for Oral Solution 100 mg which is being recalled should return it to their place of purchase.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Dr. Reddy’s Laboratories Inc
Brand name: Dr. Reddy’s
Product recalled: Sapropterin Dihydrochloride Powder for Oral Solution 100 mg
Reason of the recall: Decreased Potency
FDA Recall date: April 23, 2024

Source: www.fda.gov
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#recall #drugs #us

Global Mix, Inc. of New York, is recalling tejocote products to include the following brands: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra. The recalled products are labeled as tejocote root but are toxic yellow oleander. The recalled products were distributed in the following states: AL, AK, … See More
CA, CO, CT, DE, FL, GA, HI, ID, IL, IA, IN, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NM, NC, NY, NJ, ND, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV, WI, and WY through website. The recalled products were also sold via the below websites via courier direct delivery and mail order. Etsy, amazon, eva-nutrition, tejocotemexican, niwali, scienceofalpha. The recalling firm has not received any reported of illness.

Recalled Products include the following bearing below information. Product codes and expiration dates can be found on the bottom of the packaging.

Product Name: Eva Nutrition MexicanTejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Science of Alpha Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: NWL Nutra Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Niwali Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025

Per the safety alert update on 3/12/24, "The FDA continues to receive adverse event reports related to the products identified in this Safety Alert."

The recall was the result of a routine sampling program by the company which revealed that the finished products contained the yellow oleander. The company has ceased the production and distribution of the product as the company continues their investigation as to what caused the problem. Further the company is conducting comprehensive quality control and monitoring process.

Customers who have purchased these products should stop using them immediately and return them to the point of purchase for a full refund.

Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.

If you are experiencing symptoms after eating this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.

Company name: Global Mix, Inc.
Brand name: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra
Product recalled: Tejocote Dietary Supplements
Reason of the recall: Product contains toxic yellow oleander.
FDA Recall date: April 10, 2024

Source: www.fda.gov
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#recall #us

C
I received a package containing SUBGENIX BIORIBOSE. MY OLD CARD WAS BILLED FOR THIS I didn't order it. Subsequently my card was cancelled. I'm waiting for my new one. I'm 20lbs under weight, the last thing I need is a weight loss supplement.

#unorderedpackage #delivery #virginiabeach #virginia #us

T
I don't know what happened, All I know is I received an email from my credit union last week asking me if I ordered anything online, and I told them no, and then this week I get this package. The bubble envelope says Fullfillment House PO Box 5708 Tampa FL 33675

#unorderedpackage #delivery #uspostalservice #tampa #florida #us

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