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Hy-Vee

Updated: September 11, 2021 5:17 PM
Employees performing COVID-19 testing are not provided adequate PPE per CDC guidelines including: -N95 respirators. -Gloves that fit, creating a seal between the gown and hands.

Alleged Hazards: 2, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2020-12-21 See Less
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1. Customers are allowed to shop inside store without the use of face coverings. 2. No uniform method for disinfecting checkout conveyor belts after customers utilize them.

Alleged Hazards: 2, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-02-22 See Less
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The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for approximately 43 pounds of not-ready-to-eat (NRTE), heat treated, not fully cooked chicken enchilada products due to misbranding and an undeclared allergen. FSIS is issuing this public health alert out... See More of the utmost of caution to ensure that consumers with allergic reactions to soy are aware that these products should not be consumed. A recall was not requested because the chicken enchilada products are no longer available in commerce.

The NRTE product labeled as “HyVee mealtime CHICKEN ENCHILADAS” was produced on Jan. 3, 2021. The following product is subject to the public health alert: [View Label (PDF only)]

62.4-oz. (3-lbs. 14.4-oz.) heat and serve container of “HyVee mealtime CHICKEN ENCHILADAS” with lot code “21003” and “Best If Use By: 01/10/2021” date on the product label. The products bear establishment number “P51558” inside the USDA mark of inspection. These items were distributed to HyVee retail locations in Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska, South Dakota and Wisconsin.

The problem was discovered when a HyVee retail store employee identified the labeling issue and reported it to the establishment.

FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers with food allergies who have purchased these products are urged not to consume them. These products should be thrown away.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an illness should contact a health care provider.

For more info: fsis.usda.gov

Source: FSIS | Symptoms: Allergic Reaction
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In regards to Covid-19: 1. Per MN Executive Order 20-81, the employer does not enforce face coverings throughout all areas of the facility. 2. The employee break room and smaller departments in the facility are not set up for adequate social distancing. 3. The employer is not... See More notifying employees who may have been exposed to Covid-19 by other coworkers who had tested positive. 4. The employer is discouraging employees who were possibly exposed to Covid-19 to get tested if they do not have any symptoms.


Source: Osha.gov | Receipt Date: 2020-12-10
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October 2, 2020 Health: 1. Employees are exposed to the COVID-19 pandemic. Employees feel they are not allotted time to clean and disinfect equipment including the talkman a720 and Bluetooth emod. Clorox wipes are unavailable. Rideable pallet jacks and standing forklifts are not getting cleaned and disinfected... See More between shifts. About half of the warehouse employees do not wear masks anymore. Safety: 1. Forklift drivers operate at high speeds around corners. Employee maneuvers are unapproved by equipment manufacturers, for example entering/stepping on and exiting/off the electric equipment (rideable pallet Jacks, standing forklifts) while in motion. Employees hop off of electric walkers while the equipment is still moving. Employees have slipped off the walker platform and fallen. 2. Rideable pallet jacks and forklifts damaged the racks in the freezer, bakery, and ice cream areas. 3. Freezer floors are slippery and employees slip and fall. 4. The produce wet room floor doesn't drain and employees slip and fall. 5. The end of the warehouse gets the produce wet room products staged there; the warehouse doesn't drain, and puddles form. 6. Employees have been struck by forklifts. Forklifts strike other forklifts. Location: warehouse, freezer, produce wet room,


Source: Osha.gov | Receipt Date: 2020-10-02
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An employee was diagnosed with COVID-19, employees who worked in close proximity to this employee were not informed of their possible exposure to the virus.


Source: Osha.gov | Receipt Date: 2020-11-25 See Less
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Two employees who tested positive for COVID-19 are on quarantine, others who worked in close proximity to these employees have not been quarantined.



Source: Osha.gov | Receipt Date: 2020-10-19 See Less
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Seven Hy-Vee employees at Southeast 14th St. in Des Moines are out sick with some having tested positive for COVID-19, and others waiting for the results of their tests for the coronavirus.

Source: iowacapitaldispatch.com See Less
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Recent Interesting Reports

Latin Foods Market is voluntarily recalling one lot, LOTE 334 21, of Artri King Reforzado con Ortiga y Omega 3 tablets to the consumer level. FDA analysis has found the product to be tainted with diclofenac and dexamethasone. The product was distributed Nationwide in the USA, it... See More was sold online at www.latinfoods.com, and in retail stores. To date, Latin Foods Market has not received any reports of adverse events related to this recall.

Diclofenac and dexamethasone are both FDA approved drugs. Diclofenac is a non-steroidal anti-inflammatory drug (NSAID) indicated for the management of pain and arthritis and dexamethasone is a corticosteroid indicated for a variety of indications including but not limited to arthritis. The presence of diclofenac and dexamethasone in Artri King Reforzado con Ortiga y Omega 3 renders it an unapproved drug for which the safety and efficacy has not been established and, therefore, subject to recall.

Risk Statement: Consumption of undeclared diclofenac could result in serious adverse events that include cardiovascular, gastrointestinal, renal, and anaphylaxis in patients taking concomitant NSAIDs and/or anticoagulants, in those who have allergies to diclofenac, or those with underlying illnesses. Consumption of undeclared dexamethasone may lead to severe and serious adverse events such as adrenal suppression, a disorder in which the adrenal glands do not produce enough hormones, and adverse consequences can range from limited adverse consequences to death.

Artri King Reforzado con Ortiga y Omega 3 is marketed as a dietary supplement for relief of pain and inflammation associated with arthritis and osteoarthritis and is packaged in 100-count tablets per bottle within a cardboard carton, UPC 7 501031 111138. Latin Foods Market will notify all customers who ordered the product online in writing with an email instructing them to discard all recalled products after reviewing the FDA public notification link below and will post a copy of this press release on the Latin Foods Market website and in the retail stores where it was sold.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.  

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: Latin Foods Market
Brand name: Arti King
Product recalled: Artri King Reforzado con Ortiga y Omega 3
Reason of the recall: Undeclared Diclofenac and Dexamethasone
FDA Recall date: June 14, 2022

Source: fda.gov
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Price Chopper/Market 32 has issued a voluntary recall of Mount Royal Kids Citrus Foaming Hand Soap due to possible contamination with P. Aeruginosa, a microorganism found in the environment which poses a potential health risk, primarily in immunocompromised individuals.

- Mount Royal Kids Citrus Foaming Hand Soap.... See More UPC: 37432200293.

If you have the affected product, you may return it to your local store for a full refund. For more information, please check the link below or call 443-388-8485.

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.

Source: pricechopper.com
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1.5 years no tenant. Overgrown lawn, door falling off hinges. Lowering property values and turning area into ghetto See Less
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We have been without power since Monday night, this is so uncomfortable having no power along with this high heat and humidity. Even had to throw out the food in the refrigerator. We don’t even have water because of a pump that takes electricity. Thank you See Less
271


Green Pharmaceuticals Inc is voluntarily recalling lot 2373/21222 of SnoreStop NasoSpray, packaged in 0.3 FL OZ (9ml) bottles to the consumer level. FDA testing found product to contain microbial contamination identified as Providencia rettgeri. To date, Green Pharmaceuticals Inc has not received any reports of adverse events... See More related to this recalled lot.

This microorganism is rarely associated with human illness; however, in immunocompromised patients, the use of the recalled product could potentially result in severe or life-threatening adverse events such as bacteremia/sepsis, pneumonia, invasive fungal rhinosinusitis, or disseminated fungal infection. In non-immunocompromised patients, the use of the recalled product may result in infectious complications that are expected to be less severe and more readily responsive to treatment.

The product is used as a nasal spray to temporarily help stop or reduce symptoms of non-apneic snoring and is packaged in one single unit plastic bottle with a nasal pump as a delivery system. The affected SnoreStop NasoSpray lot includes the following: 2372/21222 (2373 is printed on a sticker placed on the bottom of the bottle and 21222 is on a sticker placed on the outer packaging).

The product can be identified by a clear transparent plastic box with the name SnoreStop NasoSpray. The product was distributed nationwide in health food stores and online. Green Pharmaceuticals Inc is notifying its retailers and customers by email and is arranging for return and replacement of all recalled products. Consumers and retailers that have product which is being recalled should stop using and return to place of purchase.

Consumers with questions regarding this recall can contact Green Pharmaceuticals Inc by phone at 805-388- 0600, Monday through Friday, 8 AM to 5 PM Pacific Standard Time. 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.

Company name: Green Pharmaceuticals Inc
Brand name: SnoreStop
Product recalled: Nasal spray
Reason of the recall: Due to microbial contamination identified as Providencia rettgeri.
FDA Recall date: June 09, 2022

Source: fda.gov
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Plastikon Healthcare, LLC is voluntarily recalling one (1) lot of Milk of Magnesia 2400 mg/10 mL Oral Suspension, one (1) lot of Milk of Magnesia 2400 mg/30 mL Oral Suspension, eleven (11) lots of Magnesium Hydroxide 1200 mg/Aluminum Hydroxide 1200 mg/Simethicone 120 mg per 30 mL Oral... See More Suspension, and two (2) lots of Magnesium Hydroxide 2400 mg/Aluminum Hydroxide 2400 mg/Simethicone 240 mg per 30 mL Oral Suspension to the consumer level. The products are being recalled due to microbial contamination. To date, Plastikon Healthcare has not received any reports of adverse events or injuries related to this recall.

Risk Statement: Administration or use of oral drug products with microbial contamination could potentially result in increased infections that may require medical intervention. Patients with compromised immune systems, such as patients in hospitals and nursing homes, have a higher probability of developing potentially life-threatening infections after taking a contaminated product.

Product indication, lot numbers, expiration dates, and NDC information are listed in the link below. The products are packaged for institutional use and are sold to clinics and hospitals nationwide in single use cups with a foil lid. The affected lots were distributed to Major Pharmaceuticals Distribution Center (wholesaler) between 7/1/2020 and 10/31/2021, who shipped to hospitals, nursing homes, and clinics nationwide. The products are private labeled for Major Pharmaceuticals.

Plastikon Healthcare is notifying its direct customers via a recall letter to arrange for return of any recalled product. Anyone with an existing inventory of the lots which are being recalled should stop use and distribution, and quarantine immediately. Return all quarantined product to the place of purchase. For clinics, hospitals, or healthcare providers that have dispensed product to patients, please notify patients regarding the recall.

Consumers with questions regarding this recall can contact Plastikon Healthcare by phone at (785) 330-7109 Monday through Friday from 9 am to 4 pm CST. 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.

Company name: Plastikon Healthcare, LLC
Brand name: Plastikon Healthcare, LLC
Product recalled: Milk of Magnesia, Magnisium Hydroxide/Aluminum Hydroxide/Simethicone Oral Suspension
Reason of the recall: Due to microbial contamination
FDA Recall date: June 08, 2022

Source: fda.gov
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