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Natural Balance LID Green Pea & Chicken Dry Cat Formula recalled due to Salmonella, Canada

2 years ago

Canada

Health Canada announced the recall of Natural Balance L.I.D. Green Pea & Chicken Dry Cat Formula by Natural Balance Pet Foods, Inc. due to possible contamination with Salmonella. As of June 2, 2021, the company has not received any reports of illness, complaints, or injuries in Canada.

Recalled cat formula products are:

- Natural Balance L.I.D. Limited Ingredient Diets® Green Pea & Chicken Formula Dry Cat Food- 5 LB Bag, Case Item Code: 2363300234, UPC: 2363300233, Lot 1008080 N811202-20, Best If Used by Date 10-Mar-2022.
- Natural Balance L.I.D. Limited Ingredient Diets® Green Pea & Chicken Formula Dry Cat Food- 10 LB Bag, Case Item Code: 2363300235, UPC: 2363300235, Lot 1008080 N811202-20, Best If Used by Date 10-Mar-2022.

Product packaging is teal coloured with dark blue accents and lettering. Product lot code and Best If Used by Dates are printed on each package. This information can be found on the back panel of each 5lb and 10lb bag.

These products were manufactured in the United States by Diamond Pet Foods and distributed in Canada by Natural Balance Pet Foods, Inc. The company reported that 378 units of the affected product were sold from February 2021 to April 2021 in Canada.

The recalled cat formula may be contaminated with Salmonella and there is risk of cross contamination and illness after handling the cat formula. Symptoms of Salmonella infection in cats may include vomiting, diarrhea, decreased appetite, fever, or excessive salivation. Some cats may not appear sick but can spread infection to other animals and humans in the household

Consumers should immediately stop feeding any of the cat formula affected by this recall to cats and dispose of it immediately or return it to their retailer for a refund. Natural Balance Pet Foods products are 100% guaranteed and all returned products will be refunded.

For more details of this recall check: healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75839r-eng.php

Source: Health Canada

84


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Amneal Pharmaceuticals, LLC. Bridgewater, New Jersey (Amneal), is voluntarily recalling 4 lots (see table below) of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL packaged in 80 mL, 150 mL, or 300 mL pack sizes, to the Consumer Level. Some bottles may have been overfilled which can... See More result in an over-potent dosing regimen. The affected Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL lots were distributed Nationwide in the USA directly to Wholesalers and Distributors. The Lots were distributed between 11/09/2023 and 2/20/2024. To date, Amneal has not received any reports of adverse events that have been confirmed to be directly related to this recall.

Risk Statement: Adult patients who are prescribed the maximum daily dose of up to 2 grams per day of Vancomycin Hydrochloride for oral solution, USP 250 mg/5mL, may receive up to 4 grams of oral vancomycin per day because of the overfilled bottle. Some patients with inflammatory disorders of the intestinal mucosa also may have significant systemic absorption of vancomycin. These patients may be at risk for the development of adverse reactions associated with higher doses of vancomycin oral solution. Worsening renal function could be associated with electrolyte abnormalities such as high potassium leading to cardiac arrest.

The recommended maximum daily dose allowance for this product is up to 2gm/day and patients prescribed a dosing regimen of 500 mg/10mL would exceed this daily allowance, which may be harmful to patients with renal insufficiency. The error occurred during the manual bottle filling stage of manufacturing.

Vancomycin Hydrochloride for Oral Solution, USP, 250mg/5mL, is administered orally for treatment of enterocolitis caused by Staphylococcus aureus (including methicillin-resistant strains) and antibiotic- associated pseudomembranous colitis caused by C. difficile.

The Vancomycin HCl for Oral Solution, USP, 250 mg/5mL subject to the recall, are identified by the NDC numbers stated on the product label. The following lot numbers of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL are included in this recall.

Vancomycin Hydrochloride for Oral Solution, USP, 250mg/5mL.
- Pack Size: 80 mL, Expiration Date: 09/2025, Lot: 22613003A, NDC No.: 69238-2261-3.
- Pack Size: 150 mL, Expiration Date: 09/2025, Lot: 22613004A, NDC No.: 69238-2261-7.
- Pack Size: 150 mL, Expiration Date: 09/2025, Lot: 22613005A, NDC No.: 69238-2261-7.
- Pack Size: 300 mL, Expiration Date: 09/2025, Lot: 22613005B, NDC No.: 69238-2261-5.

Anyone with an existing inventory of the product being recalled should examine the product and quarantine any of the recalled lots immediately. Retailers who have Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL, which are being recalled, should examine their inventory and cease dispensing any of the impacted lots.

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: Amneal Pharmaceuticals, LLC.
Brand name: Amneal
Product recalled: Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL
Reason of the recall: Super potent due to bottles being overfilled
FDA Recall date: March 27, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-nationwide-voluntary-recall-vancomycin-hydrochloride-oral-solution
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The Public Health Agency of Canada (PHAC) is investigating a Salmonella outbreak linked to snakes and feeder rodents across eight provinces. The outbreak has resulted in 70 confirmed cases of illness, 10 individuals have been hospitalized, and one fatality reported. The provinces affected include British Columbia (3),... See More Alberta (10), Saskatchewan (7), Manitoba (3), Ontario (32), Quebec (11), New Brunswick (1) and Newfoundland and Labrador (3).

Many of the individuals who fell ill reported direct or indirect contact with snakes and feeder rodents before their illnesses occurred. Some did not handle the animals themselves but lived in the same house where they were kept. A single common supplier of snakes or feeder rodents has not been identified, indicating that Salmonella bacteria can be found in many species of animals, including snakes and feeder rodents.

The outbreak, which spans from British Columbia to Newfoundland and Labrador, has been ongoing since February 2022. The infected individuals range in age from 0 to 96, with 19% of the cases involving children 5 years or younger.

The issue was first identified due to an increase in reports of Salmonella illnesses across Canada. Through the use of whole genome sequencing, it was determined that some illnesses dating back to 2022 were caused by the same outbreak strain as the illnesses that occurred in 2023 and 2024. The investigation is ongoing, and recent illnesses continue to be reported to PHAC.

You can get sick with Salmonella by touching reptiles and rodents, their food, and their environments and then touching your face, eyes, or mouth without washing your hands. To prevent further spread of the disease, individuals are advised to practice good hand hygiene and frequent handwashing after contact with snakes, feeder rodents, and their environments.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, 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 care.

Source: www.canada.ca/en/public-health/services/public-health-notices/2023/outbreak-salmonella-infections-linked-snakes-rodents.html
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84


Several brands of folic acid tablets have been recalled in Canada due to concerns that affected lots may exceed the acceptable intake limit for N-nitroso-folic acid. The recall involves multiple brands distributed across the country.

-Affected products
Brand: Compliments FOLIC ACID 1MG, Product Name: FOLIC ACID 1MG,... See More Market Authorization: NPN 00647039, Dosage Form: Tablet, Strength: Folate 1.0 mg, Lot numbers: 2G3115NHH
Brand: Equate FOLIC ACID 1MG, Product Name: FOLIC ACID 1MG, Market Authorization: NPN 00647039, Dosage Form: Tablet, Strength: Folate 1.0 mg, Lot numbers: 2G3115LRJ & 2G3115NHF
Brand: Health One FOLIC ACID 1MG, Product Name: FOLIC ACID 1MG, Market Authorization: NPN 00647039, Dosage Form: Tablet, Strength: Folate 1.0 mg, Lot numbers: 2G3115NJL
Brand: Nature's Bounty FOLIC ACID 1MG, Product Name: FOLIC ACID 1MG, Market Authorization: NPN 00647039, Dosage Form: Tablet, Strength: Folate 1.0 mg, Lot numbers: 2340T8130A
Brand: Pharmasave FOLIC ACID 1MG, Product Name: FOLIC ACID 1MG, Market Authorization: NPN 00647039, Dosage Form: Tablet, Strength: Folate 1.0 mg, Lot numbers: 2G3115NHG
Brand: Sisu FOLIC ACID 1MG, Product Name: FOLIC ACID 1MG, Market Authorization: NPN 00647039, Dosage Form: Tablet, Strength: Folate 1.0 mg, Lot numbers: 2G3115M1C

Consumers are advised to consult their healthcare provider if they have any health concerns related to this recall.

Return affected product to your local pharmacy or place of purchase. Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.

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: recalls-rappels.canada.ca/en/alert-recall/folic-acid-1mg-affected-lots-exceed-or-may-exceed-acceptable-intake-limit-n-nitroso
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Central Valley Ag Cooperative has voluntarily recalled its GS Hamster/Gerbil + Turmeric food due to a potential Salmonella contamination. The recall affects both animals and humans and is currently ongoing. The recalled product has been distributed in Kansas.

The recalled product is GS Hamster/Gerbil + Turmeric, sold... See More in bulk super sacks. A total of 7,464 pounds of the product, bearing the lot number B0624179808 11399 OXBOW and a best before date of 2/6/2026, have been recalled.

The recall was initiated after an ingredient in the gerbil/hamster feed tested positive for Salmonella.

The issue was discovered during routine testing by the company. The recall was initiated on February 26, 2024.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, 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 care.

Source: www.accessdata.fda.gov/scripts/ires/index.cfm?Product=206422
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Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulates in the product... See More solution. The lot was distributed nationwide to wholesalers and hospitals from June 16, 2022, through October 17, 2022. To date, Par has not received any reports of adverse events related to this recall.

Administration of an injectable product that contains particulate matter may result in local irritation or swelling in response to the foreign material. If the particulate matter reaches the blood vessels it can travel to various organs and block blood vessels in the heart, lungs, or brain which can cause stroke and even lead to death.

Treprostinil Injection is formulated for subcutaneous or intravenous infusion. The product is a prostacyclin vasodilator indicated for the treatment of pulmonary arterial hypertension to diminish symptoms associated with exercise and for patients who require a transition from epoprostenol to reduce the rate of clinical deterioration.

Treprostinil Injection 20mg/20mL (1mg/mL) is distributed in 20mL multidose vials as sterile solutions in water for injection, individually packaged in cartons under NDC #42023-206-01. Only Lot 57014, expiration date 04/2024 is affected by this recall. Vials from the affected lot bear the attached label.

Par is providing written notification to wholesale accounts and the hospital location that has received the affected lot and is arranging for the return of all existing inventory of Lot 57014 through Inmar, Inc. Wholesale distributors and hospital pharmacies that have the product being recalled should immediately discontinue the use and stop distribution immediately.

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.

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: Endo International, Par Pharmaceutical
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Product recalled: Treprostinil 20mg/20mL Injection
Reason for the recall: Potential Presence of Silicone Particulate Matter
FDA Recall date: March 12, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-pharmaceutical-issues-voluntary-nationwide-recall-one-lot-treprostinil-injection-due-potential
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received by Logistic   895 Meyerside Dr MISSISSIGA ONTARIO CANADA. JY243510U16208**** See Less


I did not order the item I received. There is no name of the company to return it to and the item is pretty much useless as it has a British plug on it. A month ago my Visa was compromised with 15 charges attempted on it. I don’t know if these 2 things are connected but I’m thinking they are See Less
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Nutraceutical Corporation has issued a nationwide recall for its Heritage Store Hydrogen Peroxide Mouthwash due to a risk of poisoning. The recall, announced by the U.S. Consumer Product Safety Commission (CPSC) was initiated due to the mouthwash containing ethanol at a concentration level that requires child-resistant packaging... See More under the Poison Prevention Packaging Act (PPPA). The packaging of the recalled products is not child-resistant, posing a risk of poisoning if swallowed by young children. To date, no incidents or injuries related to this recall have been reported.

The recall affects both Wintermint and Eucalyptus Mint flavors of the Heritage Store Hydrogen Peroxide Mouthwash. The product is packaged in dark opaque brown bottles with a white lid, featuring a pink and white label displaying the Heritage Store logo, product name, and flavor. All lots of these two mouthwashes are included in the recall, totaling approximately 102,100 units.

If you or a loved one are harmed by this product, 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: www.cpsc.gov/Recalls/2024/Nutraceutical-Recalls-Heritage-Store-Hydrogen-Peroxide-Mouthwash-Due-to-Risk-of-Poisoning-Violation-of-Child-Resistant-Packaging-Requirement
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