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Product: Milk

Updated: January 14, 2023 1:36 AM
My wonderful sweet Pit Bull was healthy 13 yrs old, she always slept with me!
I woke up in the morning after giving her a gnaws bone, ingredients from CHINA, which I was naive about at the time! When I awakened Tip wasn’t there, I got up... See More and there was vomit everywhere! I took her to the Vet immediately, they had no idea what was wrong, gave her antibiotics and anti nausea meds! Took her 3 times in 7 days, she would not eat or drink, 7th day, she died! I’m devastated! Any ingredients from China are dangerous! GNAWS made by Milk Bone but ingredients from China! See Less
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I just receive one after ordering a lap top 3 months ago from laptop sales.I also received a stupid pen instead of a laptop computer ordered through barrelmilk, NOT happy at all. See Less
1.2K


The affected product is being recalled from the marketplace because it contains milk which is not declared on the label. The recalled product has been sold online. This recall was triggered by a recall in another country. There have been no reported reactions associated with the consumption... See More of this product in Canada.

- Affected products:
Brand: Power Life by Tony Horton, Product: High Impact Plant Protein Chocolate Flavor, Size: 446 g (15.7 oz), UPC: 8 50010 86301 6, Codes: Lot #0914922

Check to see if you have recalled products; Do not consume recalled products to which you are allergic or sensitive as they may cause a serious or life-threatening reaction; Do not serve, use, sell or distribute recalled products

Recalled products should be thrown out or returned to the location where they were purchased

In case you experienced harm from allergens or undeclared ingredients, 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: Power Life Nutrition
Brand name: Power Life by Tony Horton
Product recalled: High Impact Plant Protein Chocolate Flavor
Reason of the recall: Issue Food - Allergen - Milk
CFIA Recall date: 2022-12-19

Source: recalls-rappels.canada.ca
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Power Life Nutrition of Woodland Hills, CA is voluntarily recalling a limited amount of its High Impact Plant Protein due to a labeling error. For a brief period during the manufacturing process, jars containing High Impact Whey Protein were mislabeled as High Impact Plant Protein. The mislabeled... See More product is safe to consume for consumers who ordered High Impact Whey Protein, but it does not contain an allergen declaration for the milk allergen in the product. People who have allergies to milk run the risk of serious or life-threatening allergic reaction if they consume these products. The recalled units of High Impact Plant Protein were shipped to customers who purchased High Impact Whey Protein from Power Life Nutrition’s website between October 18, 2022 through November 30, 2022. No serious adverse reactions have been reported to date in connection with this problem.

The product comes in a 50 ounce jar marked with lot #0914922 on the bottom.

The recall was initiated after it was discovered that a limited quantity of units of High Impact Whey Protein incorrectly contained the label for High Impact Plant Protein. Subsequent investigation indicates the problem was caused by an error in the manufacturer’s packaging process manufacturer.

No other lot numbers of High Impact Whey Protein or Plant Protein are impacted by this voluntary recall.

Consumers who have received units of High Impact Plant Protein marked lot #0914922 are urged to contact Power Life Nutrition to receive a prepaid return shipping label and free replacement product.

In case you experienced harm from allergens or undeclared ingredients, 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: THGH Partners LLC
Brand name: Power Life
Product recalled: High Impact Plant Protein
Reason of the recall: Undeclared Milk
FDA Recall date: December 15, 2022

Source: fda.gov
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The product being recalled is ByHeart Whole Nutrition Infant Formula, Milk Based Powder with Iron for 0-12 Months in 24 oz containers. The formula under voluntary recall was distributed directly to consumers in the U.S. and can be identified by the number on the bottom of the... See More can. Recalled product batches are 22273 C1, 22276 C1, 22277 C1, 22278 C1, and 22280 C1 printed with use by 01 JAN 24 or 01JUL 24. None of the distributed ByHeart product has tested positive for any contaminants No consumer complaints received, to date, that would indicate any illness.

Recall is not related to ByHeart’s own manufacturing facility in Reading, PA in any way; facility continues to run 24/7; re-stock expected in January.

ByHeart, a next-generation baby nutrition company, announced today that, out of an abundance of caution, it has chosen to voluntarily recall five batches of ByHeart Whole Nutrition Infant Formula due to the potential for cross-contamination with Cronobacter sakazakii. No distributed ByHeart product has tested positive for the bacteria.

Cronobacter bacteria can cause severe, life-threatening infections (sepsis) or meningitis (an inflammation of the membranes that protect the brain and spine). Symptoms of sepsis and meningitis may include poor feeding, irritability, temperature changes, jaundice (yellow skin and whites of the eyes), grunting breaths and abnormal movements. Cronobacter infection may also cause bowel damage and may spread through the blood to other parts of the body.

ByHeart owns its entire manufacturing supply chain with the exception of final canning, which is conducted by a reputable third-party packager. ByHeart is taking this precautionary measure because one test sample collected from the third-party packaging facility tested positive for Cronobacter sakazakii. All product packaged that day, and the first production on the next day, was isolated for destruction and not distributed. Out of an abundance of caution, we are now recalling all product produced during the entire production run.

Customers who purchased ByHeart product should check the bottom of the can and dispose of product from batches 22273 C1, 22276 C1, 22277 C1, 22278 C1, and 22280 C1.

If your infant is experiencing symptoms related to Cronobacter infection, 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 contact your health care provider to report their symptoms and receive immediate care.

Company name: ByHeart
Brand name: ByHeart
Product recalled: Whole Nutrition Infant Formula, Milk Based Powder with Iron for 0-12months
Reason of the recall: Potential for cross-contamination with Cronobacter Akasaki
FDA Recall date: December 11, 2022

Source: fda.gov
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Plastikon Healthcare, LLC is issuing an update to the voluntary recall initiated on June 3, 2022.  The recall has been expanded to include Lot 20076A of Magnesium Hydroxide 1200 mg / Aluminum Hydroxide 1200 mg / Simethicone 120 mg per 30 mL Oral Suspension. The products are... See More being recalled due to microbial contamination. To date, Plastikon Healthcare has not received any reports of adverse events or injuries related to this recall.

This lot was previously subject to a retail level recall and has been added to the current consumer level recall based on updated microorganism speciation data from third-party testing. The updated recall includes one (1) lot of Milk of Magnesia 2400 mg/10 mL Oral Suspension, one (1) lot of Milk of Magnesia 2400 mg/30 mL Oral Suspension, twelve (12) lots of Magnesium Hydroxide 1200 mg/Aluminum Hydroxide 1200 mg/Simethicone 120 mg per 30 mL Oral Suspension, and two (2) lots of Magnesium Hydroxide 2400 mg/Aluminum Hydroxide 2400 mg/Simethicone 240 mg per 30 mL Oral Suspension to the consumer level. 

Risk Statement: Administration or use of drug products with microbial contamination could potentially result in increased infections that may require medical intervention.  Patients with compromised immune systems, such as patients in hospitals and nursing homes, have a higher probability of developing potentially life-threatening infections after taking a contaminated product. 

Product indication, lot numbers, expiration dates, and NDC information are listed below. The products are packaged for institutional use and are sold to clinics and hospitals nationwide in single use cups with a foil lid.  The affected lots were distributed to Major Pharmaceuticals Distribution Center (wholesaler) between 7/1/2020 and 10/31/2021, who shipped to hospitals, nursing homes, and clinics nationwide.  The products are private labeled for Major Pharmaceuticals.

Product Name: Milk of Magnesia, 2400 mg / 30 mL, Oral Suspension.
Indications for Use: Occasional relief of constipation, (irregularity) in adults and children 12 years and older or for children under 12 as recommended by a doctor.
Lot/Exp: 20071A / Jul. 2022
NDC: 0904-6846-73
Packaging: Carton containing, 100 single dose cups (10 trays x 10 cups).

Product Name: Milk of Magnesia, 2400 mg / 10 mL, Oral Suspension.
Indications for Use: Occasional relief of constipation, (irregularity) in adults and children 12 years and older or for children under 12 as recommended by a doctor.
Lot/Exp: 20074A / Jul. 2022
NDC: 0904-6840-72
Packaging: Carton containing, 100 single dose cups (10 trays x 10 cups).

Product Name: Magnesium, Hydroxide 1200 mg / Aluminum, Hydroxide 1200 mg/ Simethicone 120 mg per 30 mL Oral Suspension.
Indications for Use: Relief of acid indigestion, heartburn, sour stomach, upset stomach due to these symptoms, pressure and bloating
commonly referred to as gas.
Lot/Exp: 21103A / Sep. 2023, 20046A / May 2022, 20076A / Jul. 2022, 20079A / Aug. 2022, 20080A / Aug. 2022, 20081A / Aug. 2022, 21057A / May 2023, 21059A / May 2023, 21095A / Sep. 2023, 21096A / Sep. 2023, 21099A / Sep. 2023, 21115A / Oct. 2022
NDC: 0904-6838-73
Packaging: Carton containing 100 single dose cups (10 trays x 10 cups).

Product Name: Magnesium Hydroxide 2400 mg / Aluminum, Hydroxide 2400 mg / Simethicone, 240 mg per 30 mL Oral Suspension.
Indications for Use: Relief of acid indigestion, heartburn, sour stomach, upset stomach due to these symptoms, pressure and bloating
commonly referred to as gas.
Lot/Exp: 20051A / Aug. 2022, 20088A / Sep. 2022
NDC: 0904-6839-73
Packaging: Carton containing 100 single dose cups (10 trays x 10 cups).

Company name: Plastikon Healthcare, LLC
Brand name: Major
Product recalled: Milk of Magnesia, Magnisium Hydroxide/Aluminum Hydroxide/Simethicone Oral Suspension
Reason of the recall: Microbial contamination
FDA Recall date: August 04, 2022

In case you experienced harm from any of these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Source: fda.gov
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Wilbur’s of Maine Chocolate Confections of Freeport, Maine is recalling its 8 oz resealable package of milk chocolate covered blueberries because they may contain undeclared chocolate covered almonds. People who have allergies to almonds run the risk of serious or life-threatening allergic reaction if they consume these... See More products. The recalled Milk Chocolate Blueberries were distributed throughout New England, in retail stores, and nationwide through mail orders. No illnesses have been reported to date in connection with this problem.

The product comes in Wilbur’s branded 8-ounce, resealable zippered pouch bag, with UPC # 81321300430 and an expiration date of April 5, 2023 stamped on the backside.

The recall was initiated after a customer discovered chocolate covered almonds in a package (of milk chocolate covered blueberries). The blueberry packaging does not reveal the presence of almonds. Consumers with nut allergies, who have purchased 8 oz packages of milk chocolate covered blueberries, with the best by date of 4/5/23, are encouraged to return them to place of purchase for a full refund.

Subsequent investigation indicates that the problem was caused by a temporary breakdown in the company’s packaging process. The process has been corrected and the company has instituted additional safety checks and corrective actions.

In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Wilbur’s of Maine Chocolate Confections
Brand name: Milk chocolate covered blueberries
Product recalled: Milk chocolate covered blueberries
Reason of the recall: Undeclared almonds
FDA Recall date: July 28, 2022

Source: fda.gov
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Plastikon Healthcare, LLC is voluntarily recalling one (1) lot of Milk of Magnesia 2400 mg/10 mL Oral Suspension, one (1) lot of Milk of Magnesia 2400 mg/30 mL Oral Suspension, eleven (11) lots of Magnesium Hydroxide 1200 mg/Aluminum Hydroxide 1200 mg/Simethicone 120 mg per 30 mL Oral... See More Suspension, and two (2) lots of Magnesium Hydroxide 2400 mg/Aluminum Hydroxide 2400 mg/Simethicone 240 mg per 30 mL Oral Suspension to the consumer level. The products are being recalled due to microbial contamination. To date, Plastikon Healthcare has not received any reports of adverse events or injuries related to this recall.

Risk Statement: Administration or use of oral drug products with microbial contamination could potentially result in increased infections that may require medical intervention. Patients with compromised immune systems, such as patients in hospitals and nursing homes, have a higher probability of developing potentially life-threatening infections after taking a contaminated product.

Product indication, lot numbers, expiration dates, and NDC information are listed in the link below. The products are packaged for institutional use and are sold to clinics and hospitals nationwide in single use cups with a foil lid. The affected lots were distributed to Major Pharmaceuticals Distribution Center (wholesaler) between 7/1/2020 and 10/31/2021, who shipped to hospitals, nursing homes, and clinics nationwide. The products are private labeled for Major Pharmaceuticals.

Plastikon Healthcare is notifying its direct customers via a recall letter to arrange for return of any recalled product. Anyone with an existing inventory of the lots which are being recalled should stop use and distribution, and quarantine immediately. Return all quarantined product to the place of purchase. For clinics, hospitals, or healthcare providers that have dispensed product to patients, please notify patients regarding the recall.

Consumers with questions regarding this recall can contact Plastikon Healthcare by phone at (785) 330-7109 Monday through Friday from 9 am to 4 pm CST. 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.

Company name: Plastikon Healthcare, LLC
Brand name: Plastikon Healthcare, LLC
Product recalled: Milk of Magnesia, Magnisium Hydroxide/Aluminum Hydroxide/Simethicone Oral Suspension
Reason of the recall: Due to microbial contamination
FDA Recall date: June 08, 2022

Source: fda.gov
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Albanese Confectionery Group, Inc. of Merrillville, Indiana is voluntarily recalling Albanese® Mini and Giant Peanut Butter Cups because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with... See More weakened immune systems. No illnesses have been reported to date.

Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.

This recall is a direct result of the J.M. Smucker Co. Jif® Peanut Butter recall. This product was not manufactured onsite at Albanese Confectionery Group, Inc. The products were distributed nationwide and reached consumers through select retail stores. The products are sold in bulk bins unpackaged.

Products affected by this recall:
- Rich’s Milk Chocolate Mini Peanut Butter Cups. Sold After: November 11, 2021
- Rich’s Milk Chocolate Giant Layered Peanut Butter Cups. Sold After: January 23, 2022

The full list of retailers where product was sold is available in the link below.

Customers who purchased the above listed product with the associated lot are urged to destroy the product or return it to the place of purchase for a full refund. Consumers with questions may contact the company at (219) 472-6306 Monday – Friday 7:00 AM – 4:00 PM

Company name: Albanese Confectionery Group, Inc.
Brand name: Rich’s
Product recalled: Peanut butter cups
Reason of the recall: Salmonella
FDA Recall date: May 27, 2022

Source: fda.gov
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