Product: Cereal

Updated:

Per4m Vegan Protein Powder - recalled due to undeclared Allergen, Ireland

8 months ago •source www.fsai.ie

Recall notice

The FSAI announced the recall of Per4m Vegan Protein powder because it is labeled as dairy-free and vegan and milk is not declared on the list of ingredients. This product was distributed in Ireland.

The recalled product is:
- Per4m Vegan Protein Powder - Salted Caramel Flavour, … See More
900g, Batch Code: 040223-10; best before date: 02/2025

If you have an allergy to or are intolerant of cereals containing gluten (barley) and/or fish do not eat it, it may cause a serious or life-threatening reaction.

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.

Source: www.fsai.ie
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#allergicreaction #ie #allergen

Per4m Vegan Protein Powder - recalled due to undeclared Allergen photo #1
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Lucky Charms, Walmart Neighborhood Market, 6850 Gulfport Blvd S, South Pasadena, FL 33707, United States, Walmart Neighborhood Market, 6850 Gulfport Blvd S, South Pasadena, FL 33707, United States

2 years ago •reported by user-cbfn9265

I just recently saw the news about people getting sick and I kind of wanted to report it. I'm just having digestive issues, i'm getting like severe headaches. And I didn't know maybe that was also due to it because like every time I eat it, I … See More
get like a headache. I haven't had the cereal in 3 days but I'm still having bathroom issues and headaches  | Symptoms: Other, Headache
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#luckycharms #walmart #6850gulfportboulevardsouth #southpasadena #florida #us #cereal

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Moderna Vaccine Side Effects, USA

3 years ago

Yesterday I received my first shot of Moderna at 1pm. About 15-20 minutes later I felt extremely nauseated. I did eat oat cereal a few hours before getting vaccinated so I didn’t have a completely empty stomach.

*7 hours later I had a bad headache, felt fatigued … See More
and started having bad body aches, and was super sleepy so I took a nap. By the 10th hour I had a low grade fever and the body aches continued.

*Next day which is today, I woke up feeling awful but I forced myself to get up and make it to my 8am cleaning at the dentist. When I got home I was in so much pain, it hurt to close my eyes and my tears felt like burning water, my insides felt like they were burning too. I finally decided enough was enough so I took some Tylenol which definitely helped. I took a nap and woke up feeling awful again so I took more Tylenol 5 hours after my first dose. It eventually wore off and I just felt all my symptoms return. I tried to eat a little and drink water and eventually took more Tylenol. The injection site is swollen and bruised and still hurts.

I really hope tomorrow is easier on me. My sister in law who actually had covid back in September got the vaccine same day as me and had no symptoms. The only thing she felt was pain at the injection site.

I guess everyone really is different or maybe she had no symptoms because her body already fought off Covid.

Although this absolutely sucks, I still plan on getting the second dose to keep me safe.

Source: www.reddit.com  | Symptoms: Body Ache, Nausea, Fever, Headache, Fatigue, Swelling
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#modernacovid19vaccine #covid19vaccine #us #cereal

303

Recent Interesting Reports

Medline and Centurion Convenience kits - recalled due to lack of sterility, USA

2 weeks ago •source www.fda.gov

Recall notice

In direct response to the Nurse Assist, LLC voluntary product recall initiated on November 6, 2023, for saline and sterile water medical products, Medline Industries, LP initiated a nationwide recall on November 15, 2023, for its Medline and Centurion branded convenience kits containing Nurse Assist 0.9% Sodium … See More
Chloride Irrigation USP and Sterile Water for Irrigation USP. The Nurse Assist recall was issued due to the potential for a lack of sterility, which could result in non-sterile products. Medline Industries, LP has received one adverse event associated with product manufactured by Nurse Assist.

Water-based medical products that are non-sterile and potentially contaminated could cause serious or life-threatening infections, including bloodstream, urinary tract, open wound/soft tissue, and respiratory infections. Patients who are elderly, critically ill, have weak immune systems (including newborn infants, pregnant women, and cancer patients), or have chronic diseases are particularly at risk of infection. However, other patients could also develop infections after exposure to contaminated water-based medical products.

The recall affects Medline and Centurion convenience kits that may be used at home by patients, caregivers, and home health providers, as well as convenience kits that may be used in medical settings for surgery or other medical procedures. Recalled kits include, but are not limited to, wound care kits, tracheostomy kits and catheter kits. A detailed list of recalled Medline and Centurion convenience kits, as well as an example of product labeling, can be found in the link below.

Consumers who have recalled product should stop using the product and contact Medline immediately.

Medline Industries, LP notified its direct distributors and consumers of the Nurse Assist recall by First Class Mail and email on 11/16/23, upon receipt of initial recall notification from Nurse Assist. Customers who received the recalled product were given instructions to quarantine all affected products immediately and provide Medline with a response regarding the affected quantity on hand. Upon confirmation of the affected quantity, Medline provided customers with over-labels to place on the affected inventory, with instructions for staff to remove the affected component before using the kit. The recall notification also instructed distributors and those who resold or transferred affected product to another company or individuals to notify their customers of this recall notification.

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: Medline Industries, LP
Brand name: Medline and Centurion
Product recalled: Convenience kits
Reason of the recall: The potential for a lack of sterility
FDA Recall date: April 08, 2024

Source: www.fda.gov
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#recall #medicaldevices #us

Medline and Centurion Convenience kits - recalled due to lack of sterility photo #1
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A package I didn't order, Granbury, TX, USA

3 weeks ago •reported by user-rcjd6867

Yes I had ordered a umbrella stand and it said it was delivered but I couldn't find it, but in my mailbox I found a small package from this place Lucia in Buford Ga. It's a hair clip, very pretty but I didn't order it. Lucia 4375 South Lee St Buford Ga.

#onlineshopping #scam #onlinescam #delivery #granbury #texas #us

A package I didn't order photo #1
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3 month wait for joggers, England, UK

6 days ago •reported by user-nwmyh313

Received the most awful, cheap jogging bottoms, that cost £36 +pp from a website that no longer exists. I've seen the same pair since on Temu, selling for £4!!! Problem is, they sat with this shipping service called MPAY UK, for so long, I couldn't return them … See More
to the seller, or contact the seller, because they no longer existed, absolute scam, and this dispatch centre totally in on it!!!
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#scam #england #gb

3 month wait for joggers photo #1
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AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence, USA

3 weeks ago •source www.fda.gov

Recall notice

Eugia US LLC (f/k/a AuroMedics Pharma LLC) has initiated a voluntary recall of lot number 3MC23011 of Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial) - 10mL Vial to the consumer level due to a customer product complaint for the presence of white particles floating … See More
inside of the vial.

Administration of an injectable product that contains particulate matter may result in local irritation or swelling. If the particulate matter reaches the blood vessels or is injected intravascularly 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. To date, Eugia US LLC has not received any reports of adverse events related to this recall.

Methocarbamol injection USP 1000 mg/10 mL (100mg/mL), is used as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. It is packaged in 10 mL and packed as 25 (vials) X 04 (Printed E-Flute cartons) X 01 (Shipper) with NDC code as 55150-223-10. Eugia US LLC shipped the entire lot to wholesalers nationwide from Jan 12, 2024, through Jan 16, 2024.

The product can be identified by product name on carton and vial label and with lot number 3MC23011 and Exp. Date: Nov 2026 (NDC 55150-223-10) (See enclosed vial label). The product label is as shown in the image below.

Eugia US LLC (f/k/a AuroMedics Pharma LLC) is notifying its distributors by recall letters and is arranging for the return/replacement of all recalled products. Wholesalers, hospitals, pharmacies, institutions, and doctors with an existing inventory of the recalled product lot should discontinue use, stop distribution and quarantine the product immediately. If you have further distributed the recalled product lot, notify your accounts and/or any additional locations which may have received the recalled product. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall.

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.

If you are experiencing any harm after using this product 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 attention.

Company name: Eugia US LLC
Brand name: Eugia US LLC
Product recalled: Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial)
Reason of the recall: Device & Drug Safety – Presence of Particulate Matter
FDA Recall date: March 28, 2024

Source: www.fda.gov
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#drugs #recall #us

AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence photo #1
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