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Starbucks, Symons Valley Road Northwest, Calgary, AB, Canada
Total all time reports: 1
Latest report: March 23, 2020 9:34 PM
Starbucks drive-thru person not wearing gloves passed me my cup by holding it at the lid.
March 23, 2020 9:34 PM
“The person who gave me my coffee handed it to me with her hand gripping the lid, no gloves. I thought this was quite careless. ”
Beef jerky had some powdery substance in it, ALDI, 9021 US Hwy 19 N, Pinellas Park, FL 33782, United States
ALDI, 9021 US Hwy 19 N, Pinellas Park, FL 33782, United States
June 5, 2020 7:57 PM
“I bought some beef jerky from there and it's definitely not good and it's got a weird powdery substance in it. I returned it and looked at the rest of their stock on the same item. The rest looked fine ”
Wong's Asian Cuisine, West Main Street, League City, TX, USA
May 25, 2020 11:14 AM
“I ordered it this weekend and I was reheating it to eat now. I’m so disgusted I found a stir fried bug in it and I’m terrified to think I could have already eaten another. I threw everything away. ”
Ideal Foods Meat and Poultry Flatbread Pizza - recalled due to they were produced without benefit of inspection, California, USA
May 12, 2020 9:35 PM
“The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced the recall of approximately 3,302 pounds of meat and poultry flatbread ... /product/pizza#scroll" title="Product: Pizza">pizza products by Ideal Foods that were produced, packed, and distributed without the benefit of federal inspection. There have been no confirmed reports of adverse reactions related to this recall to date.
The recalled products were produced on various dates from October 2019 to April 2020 and bear establishment number “EST. 45351A” or “P-45351A” inside the USDA mark of inspection. These items were shipped to a distributor and retail locations in California.
- 13.5-oz. plastic-wrapped cardboard trays containing “culinevo Artisan Style Flatbread Pizza CARNE ASADA”.
- 13-oz. plastic-wrapped cardboard trays containing “culinevo Artisan Style Flatbread Pizza CHICKEN SPINACH ARTICHOKE”.
- 16.5-oz. plastic-wrapped cardboard trays containing “culinevo Artisan Style Flatbread Pizza SIZZLIN JALAPEÑO”.
- 14.5-oz. plastic-wrapped cardboard trays containing “culinevo Artisan Style Flatbread Pizza MEAT LOVERS”.
FSIS advises consumers who have purchased these products not to consume them. These products should be thrown away or returned to the place of purchase.
Check the full recall details on the FSIS website fsis.usda.gov
Source: FSIS ”
ALDI, 16 Wandella Rd, Miranda NSW 2228, Australia
April 20, 2020 4:48 AM
“Tonight I ate a pink lady apple purchased in a pack on Sunday from here.
The last two bites I took, tasted like chemicals had been injected into the apple. Tasted like poison. I immediately spat it out. My mouth felt dry afterwards.
I'm feeling ok but am very concerned. ”
McDonald's, North Reed Avenue, Reedley, CA, USA
April 17, 2020 11:57 PM
“I didn’t eat it but my Mcchicken had a black sliver in it and this was going to be eaten by my grandma and I went to have it replaced but they gave me the same ... felyhq.com/product/burger#scroll" title="Product: Burger">burger but took out the sliver after five people touching it too and tried to pass it off as a fresh burger and I have pictures of before and after but I don’t know how to attach pictures ”
Symptoms: Headache Fatigue Body Ache
Wendy's, 1829 Mangum Road, Houston, TX, USA
March 27, 2020 6:34 PM
“I had a milk shake and spice ... title="Product: Chicken sandwich">chicken sandwich. The next day I felt really tired and sore like I had the flu. My legs were aching and my head was aching and I felt like I had no energy. This lasted for 24hours I took ibuprofen. then I took some heavy metal detox and after taking the heavy metal detox the flue like symtoms completely disappeared. ”
Slaughtered cow had T B, but still sent out. Packaged for sale., double j signature cuts, West Main Street, Pierce, CO, USA
double j signature cuts, West Main Street, Pierce, CO, USA
March 27, 2020 4:12 AM
“Couple months ago Double J slaughtered a cow that had T B. An employee stated that USDA stamped it ok. It got sent out. Packaged for sale. Packing place is in pierce colo. And Swift packing in Greeley is very unclean. Unsafe. ”
Latin Cafe 2000 - Brickell, Brickell Plaza, Miami, FL, USA
March 14, 2020 4:21 PM
“Roach in my soup. A ROACH. ”
The Radisson in Covington Ky , had a roach crawl across the table today. , Eighteen at the Radisson, West 5th Street, Covington, KY, USA
Eighteen at the Radisson, West 5th Street, Covington, KY, USA
March 12, 2020 8:47 PM
“We set down and ordered our drinks and when the waiter set down the menus the roach crawled across the table ”
McDonald's, 20 Riverglen Dr SE, Calgary, AB T2C 3H8, Canada
June 11, 2020 12:00 PM
“An McDonald's employee at the Riverglen Drive location has tested positive for COVID-19. The employee worked their last shift on June 6. If you visited the restaurant recently, please report it and any other location that you visited.
Source: ... 660citynews.com ”
Recent Interesting Reports
Natural Balance Ultra Premium Chicken & Liver Paté Formula - recalled due to elevated levels of choline chloride, USA
July 6, 2020 11:30 PM
“Company name: J. M. Smucker Company
Brand name: Natural Balance
Product recalled: Ultra Premium Chicken & Liver Paté Formula
Reason of the recall: Due to elevated levels of choline chloride
FDA R ... ecall date: July 03, 2020
Recall details: The J. M. Smucker Company today announced a voluntary recall of one lot of Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food due to health concerns likely associated with elevated levels of choline chloride. Ingesting impacted product may cause nausea with excessive salivation, constricted pupils and poor vision, diarrhea or vomiting to more severe symptoms including difficulty walking, muscle shaking, tremors, irregular heartbeat, difficulty breathing, possible cardiac or respiratory failure and, in extreme situations, death. Pet parents are encouraged to contact their cat’s veterinarian immediately if their cat is displaying any of these symptoms.
If pet parents have any product matching the following description in their possession, they should stop feeding it to their cats and dispose of the product. This information can be found on the bottom of each can.
- Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food (5.5 oz). UPC: 2363353227. Lot code: 9217803. Best by: 08 04 2021
These products are most commonly sold in pet specialty retailers and online throughout the United States and Canada. No other Natural Balance® products are impacted by this recall.
The Company has received reports of adverse reactions. Pet parents that have questions or would like to report adverse reactions should call 888-569-6828, Monday through Friday, 8 a.m. – 5 p.m. ET or email anytime at firstname.lastname@example.org.
Check the full recall details on fda.gov
Source: FDA ”
Infusion pumps and sets - recalled due to pumps may not deliver fluid at the accuracy specified in the instructions, USA
April 29, 2020 7:00 PM
“Company name: CME America
Brand name: CMEAmerica BodyGuard
Product recalled: Infusion pumps and infusion sets
Reason of the recall: pumps may not deliver fluid at the accuracy specified in the instructions for use and infusion sets may under-deliver fluids
FDA Recall date: April 29, 2020
Recall ... details: CME America, a wholly owned subsidiary of BD (Becton, Dickinson and Company), a leading global medical technology company, today issued the following update regarding two previously announced voluntary recalls, one related to all models of CMEAmerica BodyGuard® infusion pumps (FDA Recall Number: Z-1474-2020) and the other related to one of the device's infusion sets (FDA Recall Number: Z-1442-2020). Both previously announced recalls have now been designated as Class I recalls by the U.S. Food and Drug Administration (FDA), which means the FDA believes that there is a reasonable probability that use of the recalled product(s) will cause serious adverse health consequences or death.
CME America previously notified customers affected by each recall and provided guidance on the potential impact to device performance when the affected products were used. Today, the company has issued an updated customer letter with additional guidance and to inform customers of the decision to suspend distribution of the BodyGuard® infusion pump system and to remove all existing products from the U.S. market.
The following is a summary of each individual product recall details:
CMEAmerica BodyGuard® Infusion Pump Recall
Details On Jan. 6, 2020, the company initiated a voluntary recall to notify customers of certain scenarios where pumps may not deliver fluid at the accuracy specified in the instructions for use that could result in a slower than expected delivery of medication (under-infusion), and/or faster than expected delivery of medication (over-infusion). Results indicate that pumps may have a delivery inaccuracy of up to ~13%. To date, no reports of patient injury has been received related to this previously announced voluntary recall. CME America has assessed the potential risks associated with the issues outlined in the initial voluntary recall and determined that the BodyGuard® infusion pump may continue to be used in certain situations in accordance with the Operator's Manual and the additional mitigations outlined in the updated customer letter until the pumps have been removed from the market.
To ensure customers retain access to critical medical equipment, particularly as the COVID-19 pandemic continues to evolve in the United States, CME America will implement a phased market removal and will continue to support the following activities in order to help limit clinical disruption and maintain patient focus during the COVID-19 pandemic: Use of products in the field in accordance with the Operator's Manual and the additional mitigations outlined in the updated customer letter; Product service and repair activities at CME America and Authorized Service Depots; and Supply of infusion sets and accessories to support the infusion pumps remaining in the field.
The BodyGuard® infusion pump is designed to deliver fluids or medications into a patient's body in controlled amounts. The pump administers fluids through an infusion tubing set into a patient's vein or through other cleared routes of administration. The system is intended for patients who require maintenance medications, PCA therapy, parenteral nutritional fluids, and general IV fluid therapy in hospital and home care environments. Typical applications for the BodyGuard® infusion pumps include but are not limited to chemotherapy, pain management, TPN, enteral nutrition fluids and antibiotics.
The recall and market removal affect approximately 28,400 devices, including all models of BodyGuard® infusion pumps listed below. These devices are primarily used in outpatient settings.
- BodyGuard 121
- BodyGuard 323
- BodyGuard 545*
- BodyGuard 575*
- BodyGuard 545 ColorVision
- BodyGuard 575 ColorVision
*Note: These two pump models were inadvertently left out of the initial customer notification
CMEAmerica BodyGuard® Microset Infusion Set Recall
Details On Sept. 16, 2019, the company initiated a voluntary recall to notify customers that certain lots of BodyGuard® Microset infusion sets, when used with the BodyGuard® infusion pump, may under-deliver fluids up to 50% at the highest flow rates. At the time of the recall, CME America informed customers in the recall announcement to discard all remaining inventory of the infusion sets (Catalog #A120-003XYVA) and committed to reimbursing impacted customers. To date, no reports of patient injury has been received related to this previously announced voluntary recall. CME America immediately stopped shipments of the affected infusion sets. This FDA classification does not change the previous guidance provided in the company's September recall announcement to customers. Affected products include:
CMEAmerica BodyGuard® Microset, Catalog #A120-003XYVA.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA ”
Williamsburg Bridge, Brooklyn, NY, USA
June 13, 2020 12:40 PM
“Peaceful protest from Manhattan to Brooklyn ”
Hardee's, Army Post Road, Des Moines, IA, USA
June 5, 2020 8:07 AM
KFC Walsall - Junction 10 M6 Services, Walsall, Wolverhampton WS2 8RL, United Kingdom, KFC Walsall - Junction 10 M6 Services, Walsall, Wolverhampton WS2 8RL, United Kingdom
KFC Walsall - Junction 10 M6 Services, Walsall, Wolverhampton WS2 8RL, United Kingdom
May 27, 2020 9:34 AM
Symptoms: Diarrhea Nausea Vomiting Lightheaded Loss of Appetite
New Jersey, USA
January 11, 2020 11:06 AM
“Thin mint hybrid vape I’ve been sick since last night around 9 ”
368-398 West Cesar Chavez Street, Austin, TX, USA
June 3, 2020 4:59 PM
“This was jun 1st. It appeared there was some kind of military on the rooftop watching. ”
Boynton Beach, FL, USA
July 6, 2020 12:53 PM
“Order from Walmart delivers. SOUTHERN HENS (frozen chicken.)
When thawed and removing giblets, to my horror, there was a brow ... le="Product: Egg">egg inside the hen!!!! The inside of the egg had dispersed but the shell was partly attached to itself. Contacted company and they told me that they had never heard of anything like this before... I have pics!!!!! Reported to Walmart and they are STILL SELLING THEM!!!!!
I would also like to name all the agencies in MS That I contacted and they kept telling me they were not responsible?!? Six Mississippi agencies where this plant is located...Yet Walmart keeps selling them!!
I called the Board of Health in Mississippi, I called the FDA, the USDA, I called Southern Hen and spoke to a person. There was no action taken, none! nobody cares that there was a frickin egg inside of a frozen hen ”
May 7, 2020 1:00 PM
“Company name: Becca Cosmetics
Brand name: Becca Cosmetics
Product recalled: Light Shifter Brightening Concealer
Reason of the recall: Potential Mold
FDA Recall date: May 07, 2020
Recall details: Company Announcement Out of abundance of caution, and in line with its commitment to consumer sat ... isfaction and safety, Becca Cosmetics is voluntarily recalling all shades of its Light Shifter Brightening Concealer because a brownish-black material identified as a common household mold was found on the sponge-tip applicator of some units. While this is unlikely to cause serious injury there is a potential risk of temporary skin and/or eye allergy and irritation.
To date, no adverse reactions or injuries have been reported. This product was manufactured in the United States and distributed nationwide. The below are the details of the product affected by this recall. No other Becca Cosmetics products are affected by this issue.
- Product Name: Becca Cosmetics Light Shifter Brightening Concealer
- Batch: 0030A, 9308A, 0052A, 0052C, 9291A, 9309A, 0036A, 0037A, 0038A, 0038B, 0041A, 9289A, 0062A, 0062B, 0062C, 9283A, 9284A, 9287A, 9288A
- Size: 3.2 mL (only size available)
- Product Description: Concealer wand with silver overlay, and a white secondary carton
- UPC: 9331137030037, 9331137030044, 9331137030051, 9331137030068, 9331137030075, 9331137030099, 9331137030082, 9331137030105
If you have this product, please stop using it and contact the place of purchase regarding a refund. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA ”
Austin, TX, USA
June 12, 2020 11:06 AM
“Starting earlier ”