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Updated: March 31, 2020 11:49 PM
Los Angeles, CA, USA
March 31, 2020 11:49 PM
“My mom has COVID-19...probably because of her job ? (I’m pissed). My dad probably has it, too, but their symptoms are very mild...supposedly because they’re vegetarians and they have strict immu ... ne support regimens. Just in quarantine at home. They should be okay but lordt ???♀️?? ”
Allergic to Meat and Given a Chicken Quesadilla, Taco Bell, 2410 East Rand Road, Arlington Heights, IL, USA
Taco Bell, 2410 East Rand Road, Arlington Heights, IL, USA
June 25, 2019 10:54 PM
“I am a vegetarian and ordered food. I was shell shocked after i received chicken ... -link" href="https://safelyhq.com/product/quesadilla#scroll" title="Product: Quesadilla">quesadilla and unknowingly i took a bite of it. On checking with the manager he told sorry and said he is not responsible for his employee mistake and said he is not sure on how to comaint this to a higher level. Also he said if anything happens to me i should come back and then sue the company.i am allergic to meats please let me know how to take this. I am feeling so pukish ”
Recent Interesting Reports
Trader Joe’s Union Square Location Temporarily Closes After Staffer Test Positive for COVID-19, Trader Joe's, 142 E 14th St, New York, NY 10003, United States
Trader Joe's, 142 E 14th St, New York, NY 10003, United States
March 25, 2020 12:39 PM
“Trader Joe’s announced that the Union Square location of its grocery store had temporarily closed for cleaning, as had the adjoining wine store, the company’s only in the city.
The staffer who tested pos ... itive at the Union Square Trader Joe’s was last in the store on Sunday, March 22, the company said. According to the store’s online hours on Google Maps, the Trader Joe’s grocery and wine stores are expected to reopen Saturday.
Source: ny.eater.com ”
KFC Chadwell Heath - Grove Farm Retail Pk, High Road, Romford, UK, KFC Chadwell Heath - Grove Farm Retail Pk, High Road, Romford, UK
KFC Chadwell Heath - Grove Farm Retail Pk, High Road, Romford, UK
May 26, 2020 3:35 AM
“Disgraceful raw chicken was totally all pink from there
what can be done about this? ”
Plymouth, MI 48170, USA
June 3, 2020 6:46 PM
“~10,000 people meet up in DOWNTOWN PLYMOUTH, Michigan at the fountain, park, marched the streets, and then city hall/police/fire Dept. started at 2pm...still happening at .7pm. Seems peaceful so far ”
Burger King, 290 S Main St, Angels Camp, CA 95222, USA, Burger King, 290 S Main St, Angels Camp, CA 95222, USA
Burger King, 290 S Main St, Angels Camp, CA 95222, USA
June 22, 2020 11:34 AM
“Thanks for serving my cousin some raw chicken meat! One bite of raw ... elyhq.com/product/chicken#scroll" title="Product: Chicken">chicken meat wont hurt right? ”
Popeyes Louisiana Kitchen, 34275 Ford Rd, Westland, MI 48185, United States, Popeyes Louisiana Kitchen, 34275 Ford Rd, Westland, MI 48185, United States
Popeyes Louisiana Kitchen, 34275 Ford Rd, Westland, MI 48185, United States
July 9, 2020 11:32 AM
“I’ve never been served a raw pizza like I was served a raw chicken sandwich ”
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 ”
Infusion System Administration Set (infusion set) - recalled due to Use of the pump system potentially could cause over-infusion or under-infusion of therapy, USA
July 8, 2020 4:00 PM
“Company name: CME America
Brand name: BodyGuard
Product recalled: Infusion System Administration Set (infusion set)
Reason of the recall: Use of the pump system potentially could cause over-infusion or under-infusion of therapy
FDA Recall date: July 08, 2020
Recall details: PRNewswire/ - CME Am ... erica, a wholly owned subsidiary of BD (Becton, Dickinson and Company), announced a voluntary recall for all CME America BodyGuard® Infusion System Administration Sets (infusion sets) used with the company's BodyGuard® infusion pumps—that were distributed beginning May 2016 (see complete impacted product list below). This action was initiated on June 16, 2020. As part of CME America's commitment to quality, following the previously announced recall (April 27, 2020) of the BodyGuard® Infusion Pump Systems, the company conducted additional flow-rate accuracy testing.
This testing revealed that some infusion sets do not meet the ±5% delivery accuracy for the system or the ±13% accuracy identified in the earlier recall notification (bd.com Therefore, the use of the pump system potentially could cause over-infusion or under-infusion of therapy and patient harm. Based on those test results CME America is providing additional information and customer actions regarding its previous recall to include all infusion sets used with the BodyGuard® infusion pump distributed beginning May 2016.
CME America has defined four categories of impacted infusion sets based on delivery inaccuracy variability, two of which (Category A and B) can continue to be used in accordance with the instructions in the recall letter (bd.com CME America also announced on April 27, 2020, the decision to suspend distribution of the BodyGuard® infusion pumps and to remove all existing products from the U.S. market. CME America will work with customers to address the latest expanded infusion set recall and will continue to maintain continuity of care during the COVID-19 pandemic. Until such time that the BodyGuard® pumps have been removed from the market, CMEA will supply accessories and infusion sets in "Category A" and "Category B" to support the infusion pumps, and customers can continue to use the products in accordance with the Operator's Manual and the additional mitigations outlined in the customer letter.
Affected Product Types:
- BodyGuard BodySet
- BodyGuard Microset with Needleless Adaptor
- BodyGuard Microsets
- BodyGuard Microset w/ Non-Vented Spike Connector
- BodyGuard set with Female Luer
- BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer
- BodyGuard Microsets with Filter
- Standard BodySet with Needleless Connectors
- BodyGuard Microset with Filter and Manual Priming Valve
- CMExpress Microbore Sets
- BodyGuard Microset with Male Luer Connectors
- CMExpress Needleless Y Site Microbore Set
Check the full recall details on fda.gov
Source: FDA ”
March 18, 2020 7:13 PM
“FDA announced the recall of Organic Kudzu Root Herbal Supplement by Mountain Rose Herbs due to the potential to be contaminated with Salmonella. No illnesses have been reported linked to this recall to date.
FDA advises consumers to discard the recalled products or return them to the place of pur ... chase. The product was distributed to customers in the US; and British Columbia, Nova Scotia, Ontario, and Quebec, in Canada.
- Organic Kudzu Root Herbal Supplement. All sizes. Lot # #24247-X / #24247.
Check the full recall on the FDA website fda.gov
Source: FDA ”
Doctor Visit: Yes
Kent Nutrition Group Home Fresh Starter AMP Crumble - recalled due to Elevated Salt Levels, Iowa, USA
May 20, 2020 11:00 PM
“Company name: Kent Nutrition Group
Brand name: Kent
Product recalled: Home Fresh Starter AMP Crumble
Reason of the recall: Elevated Salt Levels
FDA Recall date: May 20, 2020
Recall details: Company Announcement Kent Nutrition Group (KNG) of Muscatine, Iowa is voluntarily recalling 27- 25 lb.bag ... s of Home Fresh Starter AMP Crumble from a single batch due to elevated salt levels, which can present illness or death to poultry. Kent Nutrition Group has ceased distribution of this lot as FDA and the company continue their investigation. Potential health risks of elevated salt levels include decreased growth rate, increased thirst, weakness, difficulty walking, difficulty breathing and death. To date, KNG has received three complaints concerning this product, which included illnesses and deaths in broilers age 12-20 weeks. This lot was manufactured at the KNG Columbus, NE plant and includes product distributed to select DO IT® Best Hardware Stores in Oregon, Washington, California, Montana and Idaho. Product subject to the recall can be identified by product code 3487 and is identified by the lot code 1020031 stamped onto the white strip sewn used to seal the package. The company is working closely with the Food and Drug Administration (FDA) to further investigate this issue and ensure the recalled products are removed from store shelves and are no longer distributed. Customers who want Information on what to do with the product and or for more information can call Kent Nutrition Group Customer Service at 1-866-647-1212 Monday through Friday from 8 AM to 5 PM Central Time. Customers who have purchased Home Fresh Starter AMP Crumbles lot #1020031 are urged to dispose of or return it to the place of purchase for a full refund.
Check the full recall details on fda.gov
Source: FDA ”
McPherson Dillons employee tested positive for COVID-19, Dillons Food Store, 1320 N Main St, McPherson, KS 67460, USA
Dillons Food Store, 1320 N Main St, McPherson, KS 67460, USA
April 12, 2020 12:00 PM
“Details: McPherson County says the employee was not showing symptoms while on the clock, but started to feel sick and left work for the day.
Dillons says it's supporting the employee with emergency paid leave and discussed sanitation efforts it immediately took after learning of this case.
Rep ... ort: 4/10/2020
Source: kwch.com ”