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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)

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Eat Fresco Ancient Grain Jackfruit Bowl Sold at Publix - recalled because it may contain an undeclared allergen, Florida, USA

September 1, 2020 4:36 PM

Florida, United States

Fresco Foods Inc. of Tampa, FL is voluntarily recalling ALL units of Ancient Grain Jackfruit Bowl sold at Publix because it may contain an undeclared allergen, FISH (anchovies). People who have an allergy or severe sensitivity to FISH (anchovies) run the risk of serious or life-threatening allergic reaction if they consume these products.

The allergy alert was initiated after it was discovered that the Ancient Grain Jackfruit Bowl containing Fish was distributed in packaging that did not reveal the presence of fish. Subsequent investigation indicates the problem was caused by sourcing the wrong sub-ingredient.

- Eat Fresco Ancient Grain Jackfruit Bowl. GTIN: 85898800510. Lot/Exp. Date: ALL

Individuals with an allergy or sensitivity to fish (anchovies) should not consume this product. Households that include individuals with an allergy or sensitivity to fish (anchovies) should dispose of the product or return it to the place of purchase for a refund.

Consumers with questions may contact Fresco Foods, Inc. at (813) 551-2100.

Check the full recall details on corporate.publix.com

Source: Publix

Reported By SafelyHQ.com User

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January 8, 2021 6:01 PM

“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketoro... See Morelac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter. Particulate matter was found in reserve sample vials. No adverse event reports have been received for the recalled lot, which was produced and sold in 2019.

Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.

Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine Injection should not exceed 5 days. Listed below is a table of the recalled lot distributed nationwide in the United States to wholesalers, distributors, hospitals, and pharmacies between March 28, 2019 and September 3, 2019.

Product Name/Product size: Ketorolac Tromethamine Injection, USP, 30mg / mL, 1 mL fill in a 2 mL amber vial
NDC Number: 63323-162-01
Product Code: 160201
Batch Number: 6121083
Expiration Date: 02/2021
First Ship Date: 03/28/2019
Last Ship Date: 09/03/2019

Fresenius Kabi is notifying its distributors and customers by letter and asking customers and distributors to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product. Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing the affected lot, and to return the product to Fresenius Kabi.

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
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Covid-19 OSHA Complaint, Acorn Stairlifts, 7335 Lake Ellenor, ORLANDO, FL, 32809, USA

Acorn Stairlifts, 7335 Lake Ellenor, ORLANDO, FL, 32809, USA

January 13, 2021 12:00 PM

“1. The employer is not providing sanitation product in accordance with the CDC guidelines, only one bottle of Windex is present in the facility. 2. Employees are also not social distancing in the lunch area as recommended by CDC. 3. Common areas where employees are allowed to gather and/or work are... See Morenot been sanitized as recommended by CDC guidelines.

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International Flavors & Fragrances Inc., 2051 North Lane Avenue, JACKSONVILLE, FL, 32254, USA

January 13, 2021 12:00 PM

“1- Employer is not informing other employees when an employee has had Covid-19 2-An employee died from Covid-19 and it was not reported to OSHA 3- Employer is not doing a good job of contact tracing when an employee has had Covid-19 4-Trip and fall hazard located in the Terpene Department and Aromat... See Moreics Department, with the "Grape Vine" a collection of pipes hooked up to hoses.

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Source: Osha.gov | Receipt Date: 2020-12-17
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Estyle Corp, LLC, 11650 Central Pkwy, JACKSONVILLE, FL, 32224, USA

January 13, 2021 12:00 PM

“On or about December 3, 2020, there was a positive COIVD-19 case reported. Employees in the office area were tested on December 7, 2020 but four managers were not.

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Nielson, Hoover & Company, 8000 Governors Square Boulevard, MIAMI LAKES, FL, 33016, USA

January 13, 2021 12:00 PM

“The employer does not follow CDC's guidelines to prevent the spread of the virus COVID-19, such as providing the proper face covering, and enforcing the proper quarantine to those who might been infected. A possible violation of the OSH Act of1970 General Duty Clause Section 5(a)(1).

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Covid-19 OSHA Complaint, Apria Healthcare, 10385 Ironwood Road, PALM BEACH GARDENS, FL, 33410, USA

Apria Healthcare, 10385 Ironwood Road, PALM BEACH GARDENS, FL, 33410, USA

January 13, 2021 12:00 PM

“The employer does not follow CDC's guidelines to prevent the spread of the virus COVID-19, such as providing the proper personnel protective equipment to the drivers delivering medical equipment, and exposing them to be in direct contact when picking up the medical equipment used by possible COVID-1... See More9 infected patients without been prior disinfected . A possible violation of the OSH Act of1970 General Duty Clause Section 5(a)(1).

Alleged Hazards: 2, Employees Exposed: 4
Source: Osha.gov | Receipt Date: 2020-12-21
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Covid-19 OSHA Complaint, Vinylize Creation LLC, Stirling Road, Dania Beach, FL 33004, USA

Vinylize Creation LLC, Stirling Road, Dania Beach, FL 33004, USA

January 13, 2021 12:00 PM

“Employees exposed to COVID-19 due to lack of social distancing amongst 10 employees, lack of COVID-related protective practices, and lack of masks. Potential violation of General Duty Clause 5(A)(1). Location: Main building

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January 13, 2021 12:00 PM

“The employer does not follow CDC's guidelines to prevent the spread of the virus COVID-19, such as not practicing social distance (6 feet). A possible violation of the OSHA Act of 1970, General Duty Clause, Section 5(a)(1).


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Covid-19 OSHA Complaint, Florida Foot and Ankle Associates, 8200 NW 27 ST, DORAL, FL, 33122, USA

Florida Foot and Ankle Associates, 8200 NW 27 ST, DORAL, FL, 33122, USA

January 13, 2021 12:00 PM

“The employer does not follow CDC's guidelines to prevent the spread of the virus COVID-19, such as not providing soap, hand sanitizer and disinfecting products to clean the common areas, and not enforcing the proper protocol applicable to employees who might have been exposed to COVID-19. A possible... See Moreviolation of the OSH Act of1970 General Duty Clause Section 5(a)(1)

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Recent Interesting Reports

January 4, 2021 7:46 PM

“I ordered a hand held chain saw on Dec 12th 2020. I was v
Charged $40.89 .
What did come in the mail
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December 27, 2020 3:02 PM

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December 23, 2020 10:00 PM

“Company name: Shane Erickson, Inc. DBA Innovative Marketing Consultants
Brand name: IMC
Product recalled: Wash-Free Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: December 23, 2020
Recall details: Shane Erickson, Inc. is voluntarily recalling lot 2020/05/11 and MFG:... See More2020/05/10 L/N: 20200510-3 of imc Wash-Free Hand Sanitizer 50 ml, 100 ml, 300 ml and Wash Free Hand Sanitizer 300 ml lot 2020/05/11 and Thrifty White Pharmacy Wash-Free Hand Sanitizer 300 ml lot 2020/05/11 listed in the table below to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol).

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date, Shane Erickson, Inc. has not received any reports of adverse events related to the product(s) of this recall. Recalled Products:

- IMC Wash-Free Hand Sanitizer 50 ml, 1.7 oz (8 19845 00597 8). Lot: 43962. Expiration date: 45056
- IMC Wash-Free Hand Sanitizer 100 ml, 3.4 oz (8 19845 00598 5). Lot: MFG: 2020/05/10 L/N: 20200510-3. Expiration date: N/A
- IMC Wash-Free Hand Sanitizer | Wash-Free Hand Sanitizer | Thrifty White Pharmacy Wash-Free Hand Sanitizer 300 ml, 10.14 oz (8 19845 00599 2). Lot: 43962. Expiration date: 45056

The product is used as a hand sanitizer for handwashing to decrease bacteria on the skin when soap and water are not available. All products are packaged in a plastic bottle. The 50 ml are in a HDPE opaque white bottle with a blue cap, the 100 ml is in a clear PET bottle with a clear cap and the 300 ml are in a clear PET bottle with a black pump. The product can be identified by checking the product size, UPC details, lot number and expiration date on the bottle containing the product. The product can also be identified by this information on the back label: Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384, YUEWEIXIAOZHENGZI (2020) - 04 - No. 0023.

Some of the product has custom front labels (see examples below) the back label on the custom labels have the same identification information as previously mentioned above. The hand sanitizer was distributed Nationwide in the USA to wholesale and retail customers.

Shane Erickson, Inc. is notifying its distributors and customers by mail/email and is arranging for the return of all recalled products. Consumer, distributors, and retailers that have product, which is being recalled, should stop use or distribution and return to place of purchase. Consumers with questions regarding this recall can contact Shane Erickson, Inc. by phone at 952.252.1254 [Call: 952.252.1254] or email sales@imcsuccess.com Monday through Friday from 8:00 am to 5:00 pm Central Time Zone.

Check the full recall details on fda.gov

Source: FDA
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December 30, 2020 9:21 AM

“The FDA is alerting pet owners and veterinary professionals about certain Sportmix pet food products manufactured by Midwestern Pet Foods, Inc. that may contain potentially fatal levels of aflatoxin. As of December 30, 2020, 28 deaths and 8 illnesses in dogs that ate the recalled product have been r... See Moreeported. This is an ongoing investigation. Case counts and the scope of this recall may expand as new information becomes available.

Aflatoxin is a toxin produced by the mold Aspergillus flavus, which can grow on corn and other grains used as ingredients in pet food. At high levels, aflatoxin can cause illness and death in pets. Pets experiencing aflatoxin poisoning may have symptoms such as sluggishness, loss of appetite, vomiting, jaundice (yellowish tint to the eyes or gums due to liver damage), and/or diarrhea. In severe cases, this toxicity can be fatal. In some cases, pets may suffer liver damage but not show any symptoms.

Pet owners should stop feeding their pets the recalled products listed below and consult their veterinarian, especially if the pet is showing signs of illness. The pet owner should remove the food and make sure no other animals have access to the recalled product. Sanitize pet food bowls, scoops, and storage containers using bleach, rinsing well afterwards with water, and drying thoroughly. There is no evidence to suggest that pet owners who handle products containing aflatoxin are at risk of aflatoxin poisoning.

Midwest Pet Food, Inc. already recalled the following lots of Sportmix pet food products:
- Sportmix Energy Plus, 50 lb. bag. Lots: Exp 03/02/22/05/L2 | Exp 03/02/22/05/L3 | Exp 03/03/22/05/L2
- Sportmix Energy Plus, 44 lb. bag. Lot: Exp 03/02/22/05/L3
- Sportmix Premium High Energy, 50 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Premium High Energy, 44 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Original Cat, 31 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Original Cat, 15 lb. bag. Lots: Exp 03/03/22/05/L2 | Exp 03/03/22/05/L3

Check the full outbreak announcement on fda.gov

Source: FDA
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January 1, 2021 8:08 AM

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January 8, 2021 12:49 PM

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January 4, 2021 3:23 PM

“I ordered a Stihl battery powered chainsaw as.shown on the advertisement on Facebook but instead I received a Commando Wire Saw that worked manually. I feel this needs to reported if not made right! The advertisement was very misleading. See Less
Reported By SafelyHQ.com User

January 5, 2021 5:07 PM

“I ordered a Skil handheld battery operated chainsaw and after several weeks received a pocket chainsaw in a small pouch. Never in any of the advertisements for the chainsaw that I ordered were there pictures of the pocket chainsaw I received. I even used PayPal to protect myself. This is clearly a... See Morescam and they need to be held accountable. This was Christmas present for someone and not only was it late, now it's not even what I ordered!! See Less
Reported By SafelyHQ.com User

January 4, 2021 10:32 PM

“Totally false advertising. I order two chainsaws and got two open 26" chains with straps on both ends. Not happy. This advertising was misleading and took over 30 days to receive this product in the mail. I am totally dissatisfied with this purchase and company. See Less
Reported By SafelyHQ.com User