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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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Lithia Ford Lincoln of Fresno, East Auto Center Drive, Fresno, CA, USA

Total all time reports:  1
Latest report: March 30, 2020 4:04 PM
Lithia Ford Lincoln of Fresno for forbidden business activity, Lithia Ford Lincoln of Fresno, East Auto Center Drive, Fresno, CA, USA

Lithia Ford Lincoln of Fresno for forbidden business activity

March 30, 2020 4:04 PM

“This dealerships General Manager, is NOT complying with our City’s mandated Stay Home order. According to manager, dealership is Essential and he already has a sales schedule set out for March 31, 2020 - end of April 2020. This is ridiculous. This type of behavior shows ZERO REGARD for the safety o ... See Moref himself, his family, his employees or their families, including the City of Fresno. This needs to be shut down and definitely reprimanded for actions. See Less
Reported By SafelyHQ.com User

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Recent Interesting Reports

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 ... See Moreisfaction 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
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Reported By SafelyHQ.com User

March 21, 2020 3:19 PM

“Interview - Doctor in Paris, France:
This is a first-hand account from a SafelyHQ user that is a medical professional on the coronavirus situation in France. She discusses how her work has changed since the start of the pandemic, work rotations and testing for medical professionals, and issues faci ... See Moreng patients and medical professionals.

Charlotte:
I'm a pediatric resident and I work in a pediatric hospital. I was working in the genetics unit and it's mostly outpatient and non-intensive care, so we were actually closed down last week. Just because most of us are pediatricians and so we were kind of needed elsewhere. So I decided to stop working because of my pregnancy. But then all my other colleagues are still working and they're actually now, at home, confined at home and they're waiting to be called to different departments are probably either the ER or intensive care unit and from what they understand for now, they just have to stay home and rest. And they're going to be called out probably next week when the first wave of doctors start being a little tired, probably hospitalized because they themselves are sick. So right now they're mostly, resting at home. And then I know that our unit, so was shut down and a lot of other non-urgent care at our hospital was shut down and everything is being reorganized so that we have Covid units. And so at the hospital I work in, is actually a pediatric hospital, but they're going to open an adult Covid unit just because obviously adults are more affected than children are.

SafelyHQ:
Are there any changes as a pediatrician?

Charlotte:
In most maternity at least in Paris, the dads aren't allowed in the delivery room or in the hospital at all for now. So things are pretty rough on new moms right now. And I know that we're also kind of being slowly prepared that we're probably not going to be able to have an epidural just because there won't be any doctors available. So, getting prepared for maybe a rough delivery for most new moms right now, at least new Parisian moms.

SafelyHQ:
Is testing easy for people to get so far or has it been a problem for some people. And how do things look like on that front?

Charlotte:
So, in our hospital it's very easy for all medical, staff if they have any of the symptoms to get tested. It's very, very easy. I know that for patients we only test patients that are unstable or in very critical care. Just because we can't afford to test everyone, but staff is definitely prioritized and we're all told we can get tested as easily if we want to. Or if I mean, not if you want to obviously if you have symptoms.

SafelyHQ:
Did you know anyone who has got diagnosed with coronavirus?

Charlotte:
Yeah, actually, I already have a couple of friends who are staying at home because they have it. One of my, well actually he is also a pediatric resident is at home right now with, well he's getting tested today, but it's most likely Covid. His wife was tested and got tested positive after having a five day fever. And now he has a fever since yesterday, so he did his test today. So very, very likely, also Covid positive. And so his wife is also a medical resident who probably got it working at the ER and then he got it through her.

SafelyHQ:
Being in the medical field and seeing what, the medical field is doing in France and learning about, about coronavirus. And having some friends who have it, do you have any, messages that you, they have for people who want to learn more?

Charlotte:
I think just the best thing is to stay informed on what's happening on reliable sites because I know there's a lot of misinformation out there and just do what they can to stay home. Because the big wave is going to come. And I know all my friends in the hospitals are getting as ready as they can, but I'm sure you've heard that there already some parts of France that are in a very, very complicated situation where they're already out of machines for like life support machines and out of room in intensive care units. And so hopefully Paris doesn't get there, but we never know. And it all kind of just relies on people really being careful and staying home and I know everyone wants to go outside to buy their bread and whatever, but it's always a risk. And just be mindful that, yeah, doctors are doing the best they can. And I know I have friends that are pharmacist and other things like that that are complaining because they don't have masks or they're not protected. But the truth is doctors rarely have mask as well, and everyone's of kind of going through it as they can and doing the best they can. So yeah, that's the message. I think just relax, stay at home and know that everyone is trying to get organized and do the best they can, and it's obviously not perfect, but it is what it is for now.
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Reported By SafelyHQ.com User

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
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June 25, 2020 5:31 PM

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Protests, Austin, TX, USA

Austin, TX, USA

June 12, 2020 11:06 AM

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June 22, 2020 11:34 AM

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June 18, 2020 11:00 PM

“Company name: GSK Consumer Healthcare
Brand name: Robitussin
Product recalled: Cough and cold products
Reason of the recall: Incorrect dosing cups
FDA Recall date: June 18, 2020
Recall details: GSK Consumer Healthcare is voluntarily recalling to the retail level two lots (listed below) of Ch ... See Moreildren's Robitussin® Honey Cough and Chest Congestion DM and one lot of Children's Dimetapp® Cold and Cough, due to the inclusion of incorrect dosing cups. During the review of the packaging documents for these products, GSK discovered that the dosing cups for the Children's Robitussin® Honey product are missing the 5 mL and 10 mL graduations, while the dosing cups for the Children's Dimetapp® product are missing the 10 mL graduation. The dosing cups packaged with both products only have the 20 mL graduation.

There is a potential risk of accidental overdose if caregivers dispensing the syrup do not notice the discrepancies between the graduations printed on the dosing cups and the indicated amounts to be administered (as directed in the instructions for use). Children's Robitussin Honey Cough & Chest Congestion DM contains 10 mg dextromethorphan HBr USP and guaifenesin USP 100 mg per 10 mL, and is labeled for children 4 and older, as well as adults. Children's Dimetapp Cold & Cough contains 2 mg brompheniramine maleate USP, 10 mg dextromethorphan HBr USP, and 5 mg phenylephrine HCl USP per 10 mL, and is labeled for children 6 and older, as well as adults.

Symptoms of overdose of either product may include any of the following: impaired coordination; brain stimulation causing increase in energy, elevation in blood pressure, heart rate, and respiration; a lack of energy and enthusiasm; severe dizziness or drowsiness; slow heart rate; fainting; psychotic behaviour; restlessness; seizure; decreased respiration; nausea; vomiting; constipation; diarrhea; abdominal pain; visual and hearing hallucinations; urinary retention.

As of the date of the recall announcement, GSK Consumer Healthcare has not received any adverse events related to these products or consumer complaints regarding the incorrect dosing cups supplied with the product. The recall is limited to the three lots listed below:

Children's Robitussin® Honey Cough and Chest Congestion DM (4oz)
NDC 0031-8760-12
Lots: 02177 (Exp. Jan. 2022) / 02178 (Exp. Jan. 2022)

Children's Dimetapp® Cold and Cough (8oz)
NDC 0031-2234-19
Lot: CL8292 (Exp. Sep. 2021)

These lots were distributed nationwide between February 5, 2020 and June 3, 2020 within the United States. GSK Consumer Healthcare has notified wholesalers, distributors and retailers to arrange for return of any recalled product. Wholesalers, distributors and retailers with an existing inventory of the lots being recalled should stop distribution and quarantine these lots immediately.

Wholesalers, distributors and retailers that have further distributed the recalled product should notify any accounts or additional locations which may have received the recalled product from them. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. In December 2018, GlaxoSmithKline plc reached an agreement with Pfizer, Inc. to combine their consumer health businesses into a new Joint Venture. August 01, 2019 was the first day of the new GSK Consumer Healthcare Joint Venture. Thus, when identifying impacted product, please be aware the Pfizer company name will still be present on the label.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

March 25, 2020 8:31 PM

“Building management informed us that someone was confirmed tested positive in our building. See Less
Reported By SafelyHQ.com User

July 9, 2020 11:32 AM

“I’ve never been served a raw pizza like I was served a raw chicken sandwich See Less
Reported By SafelyHQ.com User

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 ... See Moreitive 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
See Less
Reported By SafelyHQ.com User