Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case!
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please provide email or phone
Please provide email or phone

We do not show your email or contact info

Please accept our Terms & Conditions
Add photos or video
We recommend photos and videos to help explain your report
Add Photo/Video
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!


IMPORTANT - Your report is queued
It may take up to 12 hours to process your report.


Email us at support@safelyhq.com if you have questions.

Report by
Loading...
Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

ALDI Advent Calendars for Cats and Dogs - recalled due to potential choking hazard, USA

2 years ago

United States

ALDI is voluntarily recalling Pure Being Cat Advent Calendars and Pure Being Dog Advent Calendars as a precautionary measure due to a potential choking hazard. After receiving a small number of customer complaints and discussion with the supplier, ALDI immediately removed the affected products from stores. The affected products are:

- Pure Being Cat Advent Calendar (5.15 oz Box). UPC: 4099100267754. Best If Used By: All
- Pure Being Dog Advent Calendar (5.15 oz Box) UPC: 4099100267747. Best If Used By: All

No other ALDI products are affected by this recall.

ALDI takes the safety and integrity of the products it sells seriously. If customers have product(s) affected by this voluntary recall, they should discard it immediately or return it to their local store for a full refund.

Customers may contact Pet Brands Products’ Customer Service at 866-396-3647 for more information.

Company name: ALDI
Brand name: Pure Being
Product recalled: Advent Calendars for Cats and Dogs
Reason of the recall: Potential choking hazard
FDA Recall date: January 04, 2022

Check the full recall details on www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/association-pet-brands-products-llc-aldi-voluntarily-recalls-pet-advent-calendars-due-potential

Source: FDA

303


Related Reports

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
See Less
303


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
See Less
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
See Less
84


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
See Less


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
Brand name: Par Pharmaceutical
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
See Less
303


A power outage was reported near Oak Hill Road in Evansville. According to CenterPoint Energy’s power outage map, at least 3,000 customers are affected. The outage started at around 7:40 a.m. Power has been restored for most of the customers in the area.

Outage link: midwest.centerpointenergy.com/outage/current
Source:... See More www.14news.com/2024/03/29/power-outage-affecting-residents-near-oak-hill-rd/
Published: 2024-03-29
See Less


Los Angeles Department of Water & Power reported about 839 customers without electricity in Sun Valley, Los Angeles on Friday morning, Mar 29. The estimated time for restoration is 8:30 a.m. PST. The cause of the outage is not listed. Crews were assigned and are working to... See More safely restore power to the area.

Outage link: www.ladwp.com/outages/power-outage-map
Source: www.ladwp.com/
Published: 2024-03-29
See Less


CenterPoint Energy reported about 483 customers without electricity in The Woodlands in Montgomery County, on Friday morning, Mar 29. The outage started at 12:14 a.m. The estimated time for restoration is 10:12 a.m. The cause of the outage was not yet determined. Crews are working to safely... See More restore power to the area.

Outage link: gis.centerpointenergy.com/outagetracker/
Source: www.centerpointenergy.com/en-us/pages/selfid.aspx
Published: 2024-03-29
See Less


El Paso Electric reported about 976 customers without electricity in El Paso, on Friday morning, Mar 29. The outage started at 9:21 a.m. The cause of the outage was not yet determined. Crews are en route to assessing the outage.

Outage link: www.epelectric.com/outage-center
Source: www.epelectric.com/
Published: 2024-03-29 See Less


Entergy Texas reported about 847 customers without electricity in Cleveland in San Jacinto County, on Friday morning, Mar 29. The outage started at 8:59 a.m. The estimated time for restoration is 11:30 a.m. The cause of the outage was not yet determined. Crews are en route to... See More assessing the outage.

Outage link: www.etrviewoutage.com/map?state=TX
Source: www.entergy.com/
Published: 2024-03-29
See Less


Recent Interesting Reports

I received Verti Bioribose from Manufactured for Verti Products in Tampa Florida 33626 sent from a Fullfillment House, PO Box 5708
1-800-609-4174
I did not order this metabolism product so why did I receive it. See Less
522


I recieved a package in the mail through USPS Ground Advantage labeled fullfilment House P.O. Box 5708 Tampa, Fl with a small white canister labeled Verti. It appears to be some sort of metabolism supplement. I did not ever order this and don''t have any See Less
266


I received a phishing email claiming to be “Malwarebytes” offering me a 3 year subscription that a) doesn’t exist and b) I never bought, and attempted to charge me over $400 including tax.

The phishing email had the phone number: 888 889-2916, which is not Malwarebytes’s official... See More support number.

The originating email does not have malwarebytes. com, the phone number is incorrect, and I never purchased malwarebytes premium. The actual malwarebytes offering is called “plus” and not “premium”, and malwarebytes does not offer a 3 year plan option, only monthly, annually, and 2 year. Even if malwarebytes did offer a 3 year plan, the total would come out to roughly $297 and not $399, since the annual option is priced at 99.99 on Malwarebytes’s website.

Per malwarebytes’s official website, renewal emails come from the following addresses, and none of them are present:
no-reply@ store-mail.malwarebytes. com
no-reply@ mail.malwarebytes. com
noreply@ e.malwarebytes. com
noreply@ t.malwarebytes. com

I already alerted both Malwarebytes and relevant regulators (FTC, FBI).
See Less
168


What a fricking joke! Ordered on Facebook a crystal window hanging. Got a half finished product with no way to hang it from the top. Way, way smaller than the picture online. Big time SCAM!!! See Less
130


I didn't get what I ordered and I pay money for it and I contact someone by email and told me that can't send me what I ordered and I say to gived me back my money o send me what I ordered and no body answers from yesterday See Less
1


I ordered 2 Ladies Bras from a seller known as Mamoby Pte,Ltd. and received a tracking number But when I tried to track there was no rfedcord of the sale or shipment. I tried to email but it mwas not sendable. Not it has been several days... See More since the pack

I believe i have been scammed by a business in Singapor calling themselves Mamoby PTe.Ltd It has been deveral weeks since the ordxer was placed . I received confrromation that the order was sent however the tracker does not reconize the tracking Number
See Less
147


I have not ordered your product but have received 2 jars. Please do not send any more!

Im in Florence, AL, USA See Less
522


I did not order this Verti powder and it came in a bubble wrap package with no receipt. Return address was Tampa Fl See Less
1


I purchases a cordless lawn trimmer paid 38.90 plus tax was charge to my credit card and never received, Bye a cordless Lawn Trimmer on July 9 2023 and never received and my credit card was charge See Less


I paid for a package they deducted it from my card and I haven't received anything, I demand my money back See Less


Last 30 days