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1701 Wewatta Street, Denver, Colorado, United States

Updated: June 30, 2022 12:00 PM

Recent Interesting Reports

The Washtenaw County Health Department and the Washtenaw County Parks and Recreation Commission announced that Independence Lake beach has been closed for swimming the due to high levels of E. coli bacteria. The beach will reopen once follow-up tests confirm levels are low enough to safely swim... See More again.

According to the news this is the third time officials have closed Independence Lake beach this summer due to high levels of E. coli bacteria

Source: clickondetroit.com
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Random package from 188 S Mountain House Parkway. Never ordered this. Nothing else inside but this random bracelet? Odd. See Less
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Item was arrived 07-30 -22 Teterboro. I didn’t receive my order from Jlo Beauty tracking number should is in Teterboro since 7-30-22. Tracking number is 9261290278840003. See Less
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Driver illegally parks in a NO STOPPING ANYTIME spot on the Embarcadero in San Francisco during RISH HOUR TRAFFIC blocking the turning lane wasting everyone’s time because he couldn’t legally park 100
No one should be so inconsiderate that they illegally park during horrible rush hour traffic... See More when there is LEGAL parking 100 feet away. The driver refused to move his truck saying he had to park there. WTF? Blocked the turning lane for not just a couple of minutes but for at least 30. Rude Rude Rude. It’s hard enough having to driving home on a busy Friday afternoon but one of your drivers illegally parking his Amazon Delivery truck right in front of a NO STOPPING ANYTIME sign deserves to be reprimanded. You know it’s BS and all the people he held up know it too. license # 45675K3 See Less
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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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Smyrna, TN, Vi-Jon, LLC is expanding its voluntary recall to include all lots of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry to the consumer level.  This expansion includes all lots of Cherry Flavor and Grape Flavor of Magnesium Citrate Saline Laxative Oral Solution,... See More 10 FL OZ (296 mL)  within expiry. On July 14, 2022, Vi-Jon, LLC recalled all lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor, 10 FL OZ (296 mL) within expiry. The product was distributed Nationwide to wholesale and retail outlets. To date, Vi-Jon, LLC is aware of 3 (three) reports of serious adverse reactions potentially related to this recall.

Immunocompromised patients, who consume this product, may be at increased risk for invasive infections caused by Gluconacetobacter liquefaciens that could lead to serious, life-threatening adverse health consequences. The recall was initiated after Vi-Jon, LLCs third party microbial testing identified the presence of Gluconacetobacter liquefaciens. Vi-Jon, LLC is continuing their investigation into the cause of the problem.

The product is used for relief of occasional constipation (irregularity) and generally produces bowel movement in ½ to 6 hours. The product is packaged in a 10 oz clear round plastic bottle. In addition to the lemon flavor, the recall now includes the Cherry flavor and Grape flavor noted below in the table in bold print. Affected Brand, NDC #, UPC # information are listed in the link below.

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.

Company name: Vi-Jon, LLC
Brand name: Multiple Brands
Product recalled: Magnesium Citrate Saline Laxative Oral Solution
Reason of the recall: Potential Gluconacetobacter liquefaciens contamination
FDA Recall date: July 26, 2022

Source: fda.gov
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459


Edgewell Personal Care Company (NYSE: EPC) today issued a voluntary nationwide recall of three batches of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 to the consumer level as outlined in the list below. An internal review found that some samples of the product contained trace... See More levels of benzene. While benzene is not an ingredient in any Banana Boat products, the review showed that unexpected levels of benzene came from the propellant that sprays the product out of the can. To date, Edgewell has not received any adverse events related to this recall. The products were distributed nationwide in the United States through various retailers and online. Edgewell has notified its retailers to remove any remaining recalled product from shelves.

Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it potentially can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life threatening. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. Daily exposure to benzene in the recalled products would not be expected to cause adverse health consequences according to an independent health assessment using established exposure modeling guidelines.

Importantly, no other batches of Hair & Scalp (either before or after these batch codes) and no other Banana Boat products are in the scope of this recall and may continue to be used by consumers safely and as intended.

UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 20016AF, Expiration: December 2022, Size: 6 oz
UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 20084BF, Expiration: February 2023, Size: 6 oz
UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 21139AF, Expiration: April 2024, Size: 6 oz

The voluntarily recalled sunscreen spray products are packaged in aerosol cans. Banana Boat will also offer reimbursement for consumers who have purchased a product marked with one of the lot codes in the table above. Lot codes are located on the bottom of the can. Consumers should stop using the affected product immediately and appropriately discard.

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.

Company name: Edgewell Personal Care Company
Brand name: Banana Boat
Product recalled: Hair & scalp sunscreen spray
Reason of the recall: Due to presence of benzene
FDA Recall date: July 29, 2022

Source: fda.gov
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Ultra Supplement LLC is voluntarily recalling lot number DAP272109, exp 4/1/26 of Sustango capsules packaged in 10-count blisters packaged in a carton to the consumer level. Ultra Supplement was notified by Amazon that laboratory analysis has found the product to be tainted with tadalafil, an ingredient in... See More FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. The product was distributed via the internet and fulfilled by Amazon at www.amazon.com nationwide in the USA. To date, Ultra Supplement has not received any reports of adverse events related to this recall.

On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.

The presence of tadalafil in Sustango makes this product an unapproved drug for which the safety and efficacy has not been established and therefore, subject to recall.

Consumers with underlying medical issues who take Sustango capsules with undeclared tadalafil may experience health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. The product is marketed as a dietary supplement for male enhancement and is packaged in 10-count blisters packaged in a carton, ASIN X0024468I9. The affected cartons include Lot DAP272109, Exp. 4/1/26. The product can be identified by the label below.

Ultra Supplement is notifying its distributors and customers by this press announcement and by Amazon Messaging and is arranging for return of all recalled products. Consumers that have Sustango capsules Lot# DAP272109 should stop using the product.

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.

Company name: Ultra Supplement LLC
Brand name: Sustango
Product recalled: Dietary Supplement for Male Enhancement
Reason of the recall: Undeclared Tadalafil
FDA Recall date: July 25, 2022

Source: fda.gov
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