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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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Arby's, 14020 23 Mile Road, Shelby, MI 48315, USA

Total all time reports:  1
Latest report: June 2, 2020 9:35 PM
Flat out raw chicken, Arby's, 14020 23 Mile Road, Shelby, MI 48315, USA

Flat out raw chicken

June 2, 2020 9:35 PM

“they sold me flat out raw chicken , the staff is a bunch of kids who do not care always out side talking to friends and playing with there cars See Less
Reported By SafelyHQ.com User

Related Reports

July 7, 2020 12:00 PM

“An employee at Arby’s restaurant on East M-21 in Caledonia Township has tested positive for Covid-19 on June 26. If you visited the restaurant location during that time, please report it and any other location that you visited.

Source: mlive.com ... See More See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Holiday Inn Detroit Northwest - Livonia, 17123 N Laurel Park Dr, Livonia, Michigan 48152, USA

Holiday Inn Detroit Northwest - Livonia, 17123 N Laurel Park Dr, Livonia, Michigan 48152, USA

August 11, 2020 12:00 PM

“1. Housekeepers are not wearing masks, gloves, or any PPE.
2. Housekeepers are not social distancing.
3. Staff temperatures are not being taken.
4. Staff who were potentially exposed to COVID by family members did not stay home to quarantine and came to work.
5. Potentially exposed staff not per ... See Moremitted to self-quarantine for two weeks.



Source: Osha.gov | Receipt Date: 2020-07-16
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Subway, 107 E Main St, Otisville, Michigan 48463, USA

Subway, 107 E Main St, Otisville, Michigan 48463, USA

August 11, 2020 12:00 PM

“1. My employer is not enforcing the governor's executive order 147. My employer is not requiring staff or patrons to wear a face mask. I have had to discontinue my work shifts because it is an unsafe environment.




Source: Osha.gov | Receipt Date: 2020-07-13 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, McDonald's, 1020 S State St, Big Rapids, Michigan 49307, USA

McDonald's, 1020 S State St, Big Rapids, Michigan 49307, USA

August 11, 2020 12:00 PM

“1. An employee has been diagnosed with COVID-19 and the employer isn't quarantining those who worked with the person to potentially stop spread.




Source: Osha.gov | Receipt Date: 2020-07-06 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, AMAZON, 4500 68th St SE, Caledonia, Michigan 49316, USA

AMAZON, 4500 68th St SE, Caledonia, Michigan 49316, USA

August 11, 2020 12:00 PM

“1. Employees have received multiple text messages from the facility saying 3 people have tested positive for COVID-19 and nothing has been done about it such as closing down and cleaning for 2 days.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-07-07 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, United States Postal Service, 225 Michigan St NW, Grand Rapids, Michigan 49501, USA

United States Postal Service, 225 Michigan St NW, Grand Rapids, Michigan 49501, USA

August 11, 2020 12:00 PM

“Employees in the processing areas of the facility are not required to wear face masks while inside the building.

Alleged Hazards: 1, Employees Exposed: 50
Source: Osha.gov | Receipt Date: 2020-07-20 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Little Caesars Pizza, 725 28th St SW, Wyoming, Michigan 49509, USA

Little Caesars Pizza, 725 28th St SW, Wyoming, Michigan 49509, USA

August 11, 2020 12:00 PM

“1. The employer recently wasn?t providing face masks nor requiring that employees wear one during the COVID-19 pandemic.

2. The employer is charging the employees for masks.




Source: Osha.gov | Receipt Date: 2020-07-09 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Buffalo Wild Wings, 2720 44th St SW, Wyoming, Michigan 49519, USA

Buffalo Wild Wings, 2720 44th St SW, Wyoming, Michigan 49519, USA

August 11, 2020 12:00 PM

“1. An employee has tested positive for COVID-19, and affected employees have yet to be notified by the employer. The employer is only requiring those employees to not work until they have their test results back. The employer has failed to inform employees about the current situation, even though ... See Moremany have been put at risk by working with several employees who had contact with the positive individual.
2. The employer is failing to follow CDC requirements that were established for re-opening restaurants.
3. Employees are failing to use masks, management is failing to use masks and only do so when in the front of the restaurant.
4. Employees who are working the food line, and getting sides such as celery and carrots are not using gloves but instead using their bare hands. The employer has not implemented the rule of washing hands every 30 minutes.
5. No rules are being followed at this location and even with this outbreak within the restaurant, they are not enforcing rules or shutting down to create a new plan.



Source: Osha.gov | Receipt Date: 2020-07-10
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Reported By SafelyHQ.com User

August 9, 2020 12:00 PM

“An employee at Springs Ministries at the Good News Christian Camp in Gladwin positive for the coronavirus and now 50 coronavirus cases have been linked to the camp.

Source: 9and10news.com See Less
Reported By SafelyHQ.com User

Employee test positive for Covid-19, Grosse Pointe Shores Pool, 800 Lake Shore Rd, Grosse Pointe Shores, MI 48236, USA

Grosse Pointe Shores Pool, 800 Lake Shore Rd, Grosse Pointe Shores, MI 48236, USA

August 9, 2020 12:00 PM

“A lifeguard who last worked at the Grosse Pointe Shores Pool has tested positive for the coronavirus. The employee last worked on Friday, July 24.

Source: grossepointenews.com See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

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 ... See Moredetails: 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
- CMExpress

*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
See Less
Reported By SafelyHQ.com User

Peaceful Protest, Long Island City, Queens, NY, USA

Long Island City, Queens, NY, USA

June 6, 2020 1:16 PM

“Peaceful Black Lives Matter protest at Gantry Plaza See Less
Reported By SafelyHQ.com User

August 1, 2020 5:01 PM

“Company name: Laboratorios Jaloma S.A. de C.V.
Brand name: Jaloma
Product recalled: Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: August 01, 2020
Recall details: LABORATORIOS JALOMA S.A. de C.V. is voluntarily recalling all lots and all bottle sizes of the Jaloma An ... See Moretiseptic Hand Sanitizer, Ethyl Alcohol 62% With vitamin E to the consumer level. This recall has been initiated because FDA sampled the 500 mL product and found it to be contaminated with undeclared methanol (wood alcohol). Although the contamination was linked to the 500 mL product, due to the abundance of caution, Jaloma is recalling all lots of all sizes within expiry. The NDCs, lot #s, and expiration dates are listed in the table below.

Risk Statement: Substantial methanol exposure could result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, and 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, LABORATORIOS JALOMA S.A. de C.V. has not received any reports of adverse events related to this recall.

Recalled Products:

-Product(s): Jaloma Antiseptic Hand Sanitizer Ethyl Alcohol 62% With vitamin E
-NDCs: 65055-600-02
-Sizes: 16.9 fl oz. (1.06 pt) (500 mL)
-UPC: 7 59684 51503 3
-Lot #s & Expiration Dates: 0005295 Exp: April, 2022 / 0006373 Exp: May, 2022

-Product(s): Jaloma Antiseptic Hand Sanitizer Ethyl Alcohol 62% With vitamin E
-NDCs: 65055-600-01
-Sizes: 4 fl oz (120 mL)
-UPC: 7 59684 51502 6
-Lot #s & Expiration Dates: 0005412 Exp: April, 2022 / 0007134 Exp: May, 2022 / 0007834
-Exp: May, 2022 / 0009239 Exp: June, 2022

The product is used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The products are distributed in a 4 fl oz (120 mL) Polyethylene Terephthalate (PET) plastic bottle and a 16.9 fl oz (1.06 pt) (500 mL) PET or High-density polyethylene (HDPE) plastic bottle. Product is labeled with a red logo with the word Jaloma written in white letters. The product was distributed throughout the United States. It was imported to one (1) wholesaler and two (2) distributors.

Each product contains a lot number and expiration date stamped directly on the bottle or on the label of the 16.9 fl oz HDPE bottle in the format below. See table for lot numbers of each individual bottle.

0007834 EXP0522

LABORATORIOS JALOMA S.A. de C.V. is notifying its customers/distributors by recall letter and consumers via this press release. LABORATORIOS JALOMA S.A. de C.V.is arranging for return and refund of all recalled products.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

Dead cockroach in my food, El Tapatio Dos Mexicanos Grill, East Pomona Street, Santa Ana, CA, USA

El Tapatio Dos Mexicanos Grill, East Pomona Street, Santa Ana, CA, USA

July 28, 2020 12:47 PM

“I almost ate a dead cockroach that was mixed into my camarones a la diabla. So lucky I looked before I took the bite 🤮 they didn’t refund my whole order that was made in the same kitchen, gross!!! See Less
Reported By SafelyHQ.com User

April 23, 2020 8:51 AM

“At least 6 employees at this location have tested positive for COVID 19. 5 other area awaiting results. If you were at this location within the last 2 weeks, please call Metro Health to report it. See Less
Reported By SafelyHQ.com User

July 27, 2020 6:00 PM

“Company name: 4e Brands North America
Brand name: Assured, Blumen, Modesa
Product recalled: Hand Sanitizer
Reason of the recall: Undeclared Methanol
FDA Recall date: July 27, 2020
Recall details: San Antonio, Texas, 4e Brands North America is voluntarily recalling all lots of Hand Sanitizer bra ... See Morends to the consumer level. These products are being recalled due to the potential presence of methanol (wood alcohol).

Risk Statement: Substantial methanol exposure could 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.

RECALLED PRODUCTS These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. This recall now includes all product manufactured by 4e within expiration, regardless of the size, UPC, or lot number. For full details and products click the link below.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

June 22, 2020 5:43 PM

“just came to a 24 hour location and then quarter pounder is cold and raw help!!! should I be worried about food poisoning ???! This is disgusting See Less
Reported By SafelyHQ.com User

July 13, 2020 11:27 AM

“Do not order from here See Less
Reported By SafelyHQ.com User

July 16, 2020 5:32 PM

“gotta love getting raw chicken from here! absolutely shocking! at least i won’t be dying from covid...i’ll be dying from salmonella instead See Less
Reported By SafelyHQ.com User

April 12, 2020 12:00 PM

“Details: The McDonald’s on LA Highway 16 at Lockhart Road in Denham Springs has closed after an employee tested positive for COVID-19.

Report: 4/06/2020
Source: wafb.com See Less
Reported By SafelyHQ.com User