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Product: Milk

Updated: April 15, 2022 3:02 PM
The Salsa Texan of Flower Mound, Texas is voluntarily recalling all regular and burrito sized packages of tortillas labeled as Coconut Flour Tortillas and Blended Flour Tortillas because they may contain undeclared wheat and milk. The recalled tortillas were distributed nationwide through the mail, following orders made... See More via the social media platforms, Facebook and Instagram. The recalled tortillas were also sold at various Farmers Markets in Texas. Farmers Market locations include: Canton First Monday, Lucas, Texas Community Market, St. Michael’s, Red Tent Market at Willowbend, Luscombe Farm, Rockwall, Garland, and Heath.

The recalled products come in a clear plastic package marked with The Salsa Texan on the top or may be sold unlabeled. There are no best by dates or lot codes applied to the recalled product, therefore consumers should consider all Salsa Texan flour tortillas to be included in this recall.

Consumers who have purchased The Salsa Texan tortillas are urged to destroy them if they have an allergy or sensitivity to wheat or milk. Customers with Celiac disease and gluten sensitivity have confirmed illness following consumption of the recalled tortillas.

The voluntary recall was initiated after it was discovered that the tortillas were distributed in packaging that did not reveal the presence of wheat or milk. Distribution of the tortillas have been suspended until the FDA and the company are certain that the problem has been corrected.

Company name: The Salsa Texan
Brand name: The Salsa Texan
Product recalled: Tortillas
Reason of the recall: Undeclared wheat and milk
FDA Recall date: April 15, 2022

Source: fda.gov
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Plastikon Healthcare, LLC is voluntarily recalling three (3) lots of Milk of Magnesia 2400 mg/30 mL Oral Suspension, one (1) lot of Acetaminophen 650mg/ 20.3mL, and six (6) lots of Magnesium Hydroxide 1200mg/Aluminum Hydroxide 1200mg/Simethicone 120mg per 30 mL to the hospital, clinic and patient level. The... See More products are being recalled due to microbial contamination and failure to properly investigate failed microbial testing. The affected lots were distributed to Major Pharmaceuticals Distribution Center (wholesaler) between 5/1/2020 and 6/28/2021, who shipped to hospitals, nursing homes, and clinics nationwide. 

This product potentially could result in illness due to intestinal distress, such as diarrhea or abdominal pain.  Individuals with a compromised immune system have a higher probability of developing a wide-spread, potentially life-threatening infection when ingesting or otherwise orally exposed to products contaminated by micro-organisms.

To date, Plastikon has not received any customer complaints related to microbial concerns or reports of adverse events related to this recall. Product indication, lot numbers, expiration dates and NDC information are listed below. The product is packaged for institutional use and is sold to clinics and hospitals nationwide in single use cups with a foil lid. The products are private labeled for Major Pharmaceuticals.

Recalled products:

- Product Name: Milk of Magnesia 2400 mg/30 mL Oral Suspension
Indications for use: Milk of Magnesia 2400 mg/ 30 mL is indicated for the 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.
20024A/Mar 2022
20025A/Mar 2022
20041A/May 2022
NDC: 0904-6846-73
Type of Packaging: Carton containing 100 single dose cups (10 trays x 10 cups)

- Product name: Magnesium Hydroxide 1200mg/Aluminum Hydroxide 1200mg/ Simethicone 120mg per 30 mL
Indications for use: Magnesium Hydroxide 1200mg/Aluminum Hydroxide 1200mg/Simethicone 120mg per 30 mL is indicated for relief of acid indigestion, heartburn, sour stomach, upset stomach due to these symptoms, pressure and bloating commonly referred to as gas.
Lot/exp.
20042A/May 2022
20043A/May 2022
20045A/May 2022
20046A/May 2022
20047A/May 2022
21067A/Jun 2023
NDC: 0904-6838-73
Type of Packaging: Carton containing 100 single dose cups (10 trays x 10 cups)

- Product name: Acetaminophen 650mg/ 20.3mL
Indications for use: Acetaminophen 650mg/ 20.3mL indicated for temporarily relief of minor aches and pains due to, minor pain of arthritis, muscular aches, backache, premenstrual and menstrual cramps, the common cold, headache, toothache, and temporarily reduction of fever.
Lot/exp. 20040A/May 2022
NDC: 0904-6820-76
Type of Packaging: Carton containing 100 single dose cups (10 trays x 10 cups)

Plastikon Healthcare places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Plastikon Healthcare has notified 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.

Patients are advised to contact their doctor 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: Major Pharmaceuticals
Product recalled: Magnesia Oral Suspension 2400 mg/30 mL, Magnesium Hydroxide 1200mg/Aluminum Hydroxide 1200mg/Simethicone 120mg per 30 mL, and Acetaminophen 650mg/ 20.3mL
Reason of the recall: Microbial Contamination
FDA Recall date: March 24, 2022

Source: fda.gov
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433


1. CCR T8 3205(c): The employer is allowing employees who are exhibiting symptoms of COVID-19 to work which has led to others becoming infected with COVID-19. 2. CCR T8 3205(c): The employer is not providing masks for employees so as to reduce the spread of COVID-19. 3.... See More CCR T8 3205(c): The employer has not trained employees as it relates to COVID-19 prevention. 1. CCR T8 3203(a): Employees are at risk of being struck by the gate in the milking/washing bin area. The automated mechanism that raises/lowers the gate is broken, requiring employees to lower the gate manually which comes down quickly.

Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-10-06
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157


Boil Water Alerts for Businesses
World Health Products, llc. of Monroe, CT is recalling Jetfuel Diuretic UPC 859613000859, because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume this product.

The GAT Sport Jetfuel... See More Diuretic was distributed thru the GAT Sport online store, Amazon and “Nationwide” retail stores. The recalled products bear the following lot code and Expiration Date information:

Brand: GAT Sport / Jetfuel Diuretic
Product: Jetfuel Diuretic
Size: 90 ct Bottle
Lot # 2003609
Exp. Date: 6/2023

Brand: GAT Sport / Jetfuel Diuretic
Product: Jetfuel Diuretic
Size: 90 ct Bottle
Lot # 2003610
Exp. Date: 5/2023

The lot code and expiration date are located on the bottom of the container, in bottom center of the panel, as pictured below.

This recall is being initiated because the Medium-Chain Triglycerides (MCT) oil powder ingredient contains an undeclared milk allergen.

This recall is being carried out with the knowledge of the Food and Drug Administration.

To date there have been no reports of illness involving the products addressed in this recall.

Customers with a milk allergy or sensitivity who have purchased the affected product are urged not to consume it and dispose of it or return it to the point of purchase.

In case you are experience 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: World Health Products, LLC
Brand name: GAT Sport Jetfuel Diuretic
Product recalled: Diuretic
Reason of the recall: May contain undeclared milk
FDA Recall date: January 06, 2022

Check the full recall details on fda.gov

Source: FDA
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Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared milk on the labels. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume products containing milk. There have been... See More no illnesses reported to date.

During a recent FDA inspection, the firm was notified that their labels failed to disclose the presence of milk on some of their products.

The recalled products were shipped between January 2020 through November 2021 to distributors and retailers in Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Minnesota, Nevada, New Jersey, New York, North Carolina, Ohio, and Texas.

The full list of affected products is on the link below.

Lot numbers and expiration dates are found on the bottom of each container.

Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall. Nutracap will be providing corrective label stickers for product remaining in stock. Affected consumers who have purchased these products are urged to return them to the place of purchase for a full refund or they may discard the product. Your assistance is appreciated and necessary to prevent consumer illness.

Company Announcement Date: November 12, 2021
FDA Publish Date: November 12, 2021
Product Type: Food & Beverages. Allergens
Reason for Announcement: Undeclared Milk
Company Name: Nutracap Holdings, LLC
Brand Name: Multiple brands
Product Description: Dietary Supplements

Check the full recall details on the FDA website: fda.gov

Source: FDA
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433


Nutracap Holdings, LLC of Norcross, Georgia is voluntarily recalling various dietary supplements due to undeclared wheat, milk, soy and/or coconut on the labels. People who have an allergy or severe sensitivity to soy, milk, wheat, or coconut run the risk of serious or life-threatening allergic reaction if... See More they consume products containing soy, milk, wheat, or coconut.

On 11/4/2021 during an FDA inspection the firm was notified that their labels failed to disclose the presence of allergens on some of their products. The recalled products were shipped between June 4, 2020 through October 1, 2021 to distributors and retailers in Alabama, California, Florida, and Texas. There have been no illnesses reported to date.

The affected products are:

Brand: Boba Origin. Product: 100% Whey Protein Isolate. Flavor: Brown Sugar Milk, Tea, Undeclared milk, & soy. Size: 1 gallon plastic jar. Lot No. 2106263. Exp. 07/2023

Brand: Etedream. Product: Etegrow ISO. Flavor: Snicker Doodle, Undeclared milk. Size: 2gallon plastic jar. Lot No. 2106002. Exp. 06/2023


Brand: RAW. Product: Vegan Protein Flavor: Peanut Butter, Undeclared coconut. Size: 1gallon plastic jar. Lot No. 2108070, 2104340, 2102018, 2012304, 2010266, 2010102, 2007037/746, 2005132. Exp. 08/2023, 04/2023, 02/2023, 12/2022, 10/2022, 10/2022, 07/2022, 05/2022

Brand: Steel. Product: Veg-Pro Flavor: Cookies & Crème, Undeclared Wheat. Size: 64 ounce plastic jar. Lot No. 2109390, 2104333, 2011260, 2104007/1041, 2105059, 2011260/994. Exp. 09/2023, 04/2023, 11/2022, 04/2023, 05/2023, 11/2022

Brand: Vital Force. Product: PureISO. Flavor: Milk Chocolate, Cocoa, Undeclared milk. Size: 1gallon plastic jar. Lot. No. 2108191. Exp. 09/2023

Brand: Vital Force. Product: PureISO. Flavor: Creamy Peanut, Butter Vanilla, Undeclared milk. Size: 1gallon plastic jar. Lot No. 2109068. Exp. 09/2023

Lot numbers and expiration dates are found on the bottom of each container.

Retailers and distributors who have received any of these products should check inventory, immediately remove from sale and notify customers who purchased them of the recall.

This recall is being made with the knowledge of the Food and Drug Administration.

Company name: Nutracap Holdings, LLC
Brand name: Etedream, Vital Force, Raw, Boba Origin, Steel
Product recalled: Dietary Supplement Protein Powder
Reason of the recall: Undeclared wheat, milk, soy and/or coconut
FDA Recall date: November 09, 2021

Check the full recall details on fda.gov

Source: FDA
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3203: Receipt of deliveries with a non-powered rolling conveyor on milk crates poses a hazard to employees. 3241: Storage of materials on "U-Boat" carts is too high and poses a hazard to employees when parked and in use when restocking shelves. 3205: Employees are not given adequate... See More time to conduct the cleaning and disinfecting procedures outlined in the employers written COVID-19 Prevention Program.

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-08-17
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108


A boil water advisory has been issued in the city of Hudsonville.

The advisory affects all addresses on Highland Drive between Buttermilk Court and 32nd Avenue, all addresses on Buttermilk Court, and all addresses on South Buttermilk Court.

Source: fox17online.com
Source publication date: 2021 09 22 See Less
489


1. T8 CCR § 3205(c)(3)(B) - Since April, there have been employees who tested positive for Covid-19 in the workplace and Employer has not been telling anything about it to the staff. Screenings and questionnaires are done but scanners are not wiped regularly. Employees are concerned with... See More potential exposure to Covid-19 in the workplace. 2. T8 CCR § 3205(c)(8)(C) - Two employees have tested positive for Covid-19, and Employer does not have guidelines regarding sanitation and cleaning after Covid-19 exposure in the workplace. 3. T8 CCR § 3205(c)(8)(E) - Employer does not provide Personal Protective Equipment (PPE) especially when supplies ran out. 3. T8 CCR § 3205(c)(8)(E) - At the milk aisle, one fan is off and temperature is not being met, with fan wire sparking. There are leaks making the floor wet at the frozen aisle.

Alleged Hazards: 4, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-12-01
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8.3K


1. Not limiting the number of people coming into the store. 2. Not making employees wear the mask in deli or around the store. 3. Even though the employee ordered masks and is selling them, employees are told they will not be supplied masks. An employee made... See More some masks for employees to wear. 4. The store is not properly cleaned and sanitized. 5. When employees ask questions about it the employer gets mad and tells us not to worry about it. 6. Having employees stand on milk crates to reach top shelves. 7. Black mold in produce cooler that was cleaned up by an employee on their own because it go so bad. 8. Meat is just sitting in meat cooler uncovered in open containers.


Source: Osha.gov | Receipt Date: 2020-05-01
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