About Heather Davis

My high school journalism teacher lovingly labelled me a button-pusher. She wasn’t wrong. But today, I would amend that to say I’m a button-pusher with a purpose. I push the buttons of companies that think they can get away with endangering consumers to save their bottom line. I push the buttons of insurance companies that write-off the value of human life. I push the buttons of pharmaceutical corporations that lie to and endanger the public. I’m a proud button-pusher. And my clients give that button-pushing a purpose.

Entries by Heather Davis

SoloVital.com Issues Voluntary Nationwide Recall of Umary Acido Hialuronica, Suplemento Alimenticio 850 mg Capsules Due to the Presence of Undeclared Drug Ingredients: Diclofenac and Omeprazole

July 15, 2024/in Recalls from FDA/by Heather Davis

Chula Vista, CA, SoloVital.com is voluntarily recalling all lots of Umary Acido Hialuronica, Suplemento Alimenticio – 30 Capletas de 850mg to the consumer level. FDA laboratory analysis confirmed that UMARY has been found to be tainted with the drug in...

Source: Food and Drugs Administration--Recalls/Safety Alerts

Baxter Issues Urgent Medical Device Recall for Volara System Single-Patient Use Circuit

July 15, 2024/in Recalls from FDA/by Heather Davis

Baxter International Inc. (NYSE:BAX) announced today it has issued an Urgent Medical Device Recall for certain lots of the Volara system single-patient use circuit and blue ventilator adapter assembly (see Figure 1). The recall is due to reports of the...

Source: Food and Drugs Administration--Recalls/Safety Alerts

Baxter Issues Urgent Medical Device Recall for Volar System Single-Patient Use Circuit

July 15, 2024/in Recalls from FDA/by Heather Davis

Source: Food and Drugs Administration--Recalls/Safety Alerts

AB World Foods US, Inc. Recalls Al’Fez Natural Tahini Because of Possible Health Risk

July 12, 2024/in Food Safety Recalls, Recalls from FDA/by Heather Davis

AB World Foods US, Inc. of Oakbrook Terrace, Illinois, is voluntarily recalling Al’Fez Natural Tahini in 5.6oz glass jars because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infection...

Source: FDA Food Safety Recalls RSS Feed

AB World Foods US, Inc. Recalls Al’Fez Natural Tahini Because of Possible Health Risk

July 12, 2024/in Food Safety Recalls, Recalls from FDA/by Heather Davis

Source: FDA Food Safety Recalls RSS Feed

Wiers Farm, Inc Issues a Voluntary Recall on Whole and Salad Cucumbers Due to Possible Contamination with Listeria

July 12, 2024/in Recalls from FDA/by Heather Davis

Out of an abundance of caution, Wiers Farm Inc. of Willard, OH, is voluntarily recalling a limited number of whole cucumbers with a pack date of June 5, 2024 and bagged salad cucumbers with a pack date of June 5, 2024 and June 6, 2024 due to possible c...

Source: Food and Drugs Administration--Recalls/Safety Alerts

Supercore Products Group, Inc. Issues Voluntary Worldwide Recall of Hard Steel Capsules & Gold Hard Steel Plus Liquid Due to the Presence of Sildenafil and Acetaminophen

July 11, 2024/in Recalls from FDA/by Heather Davis

Atlanta, GA, Supercore Products Group is voluntarily recalling of Hard Steel Capsules & Gold Hard Steel Plus Liquid to the consumer level. FDA analysis has found these products to be tainted with Sildenafil and acetaminophen. Sildenafil is an ingre...

Source: Food and Drugs Administration--Recalls/Safety Alerts

Baxter Issues Urgent Medical Device Recall for Life2000 Ventilator Due to Potential Battery Charger Dongle Damage

July 10, 2024/in Recalls from FDA/by Heather Davis

Baxter International Inc. (NYSE:BAX) announced today it has issued an Urgent Medical Device Recall for Life2000 ventilators with an attached battery charger dongle. The recall is due to reports that the devices are not properly charging when there is d...

Source: Food and Drugs Administration--Recalls/Safety Alerts

Baxter Issues Urgent Medical Device Recall for Life2000 Ventilator Due to Potential Battery Charger Dongle Damage

July 10, 2024/in Recalls from FDA/by Heather Davis

Source: Food and Drugs Administration--Recalls/Safety Alerts

Reser’s Fine Foods Announces Voluntary Recall of Hill Country Fare Mustard Potato Salad With a Use By Date of JUL/26/24

July 2, 2024/in Recalls from FDA/by Heather Davis

Out of an abundance of caution, Reser’s Fine Foods is voluntarily recalling Hill Country Fare Mustard Potato Salad 48oz (3LB) with a Use By Date of JUL/26/24 due to the possibility of pieces of hard plastic foreign material in the package. No injuries...

Source: Food and Drugs Administration--Recalls/Safety Alerts

About Heather Davis

Entries by Heather Davis

SoloVital.com Issues Voluntary Nationwide Recall of Umary Acido Hialuronica, Suplemento Alimenticio 850 mg Capsules Due to the Presence of Undeclared Drug Ingredients: Diclofenac and Omeprazole

Baxter Issues Urgent Medical Device Recall for Volara System Single-Patient Use Circuit

Baxter Issues Urgent Medical Device Recall for Volar System Single-Patient Use Circuit

AB World Foods US, Inc. Recalls Al’Fez Natural Tahini Because of Possible Health Risk

AB World Foods US, Inc. Recalls Al’Fez Natural Tahini Because of Possible Health Risk

Wiers Farm, Inc Issues a Voluntary Recall on Whole and Salad Cucumbers Due to Possible Contamination with Listeria

Supercore Products Group, Inc. Issues Voluntary Worldwide Recall of Hard Steel Capsules & Gold Hard Steel Plus Liquid Due to the Presence of Sildenafil and Acetaminophen

Baxter Issues Urgent Medical Device Recall for Life2000 Ventilator Due to Potential Battery Charger Dongle Damage

Baxter Issues Urgent Medical Device Recall for Life2000 Ventilator Due to Potential Battery Charger Dongle Damage

Reser’s Fine Foods Announces Voluntary Recall of Hill Country Fare Mustard Potato Salad With a Use By Date of JUL/26/24

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