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

Taro Pharmaceuticals U.S.A., Inc. Issues Voluntary Nationwide Recall of Lamotrigine Tablets USP, 100 mg, 100 Count Bottles

January 10, 2020/in Recalls from FDA/by Heather Davis

Taro Pharmaceuticals U.S.A., Inc. (“Taro” or the “Company”) is voluntarily recalling one (1) lot of Lamotrigine 100 mg Tablets, Lot # 331771 (expiration date June 2021) in 100 count bottles, NDC 51672-4131-1 to the consumer level.

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

Stryker Launches Voluntary Field Action for Specific Units of The LIFEPAK® 15 Monitor/Defibrillator

January 10, 2020/in Recalls from FDA/by Heather Davis

Stryker announced today that the company is launching a voluntary field action on specific units of the LIFEPAK 15 monitor/defibrillators.

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

Libbey Glass Recalls Milk Bottles Due to Laceration Hazard

January 9, 2020/in Consumer Product Safety Commission/by Heather Davis

The bottles can break unexpectedly during use, posing a laceration hazard.

Source: Recall List

Thesaurus Global Marketing Recalls Tricycles Due to Violation of the Federal Lead Paint Ban; Risk of Poisoning; Sold Exclusively at Amazon.com (Recall Alert)

January 9, 2020/in Consumer Product Safety Commission/by Heather Davis

Paint on the canopy’s frame contains levels of lead that exceed the federal lead paint ban and tricycle components contain levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse ...

Source: Recall List

Boston Warehouse Trading Corp. Recalls Holiday Travel Mugs Due to Fire Hazard; Sold Exclusively at Meijer Stores

January 9, 2020/in Consumer Product Safety Commission/by Heather Davis

The mugs are mislabeled as microwave safe. If microwaved, the metallic print on the mug can spark, posing a fire hazard.

Source: Recall List

Mavidon Issues Voluntary Worldwide Recall of Manufactured Products Including Lemonprep® Tubes And Single Use Cups Pediaprep® Tubes And Single Use Cups Wave Prep® Tubes And Single Use Cups Cardio Prep Single Use Cups Due To Burkholderia Cepacia Contamination

January 8, 2020/in Recalls from FDA/by Heather Davis

Mavidon is voluntarily recalling all lots of products manufactured at our facility including LemonPrep®, PediaPrep® and Wave Prep 4-ounce tubes and single use cups, Cardio Prep and Collodions, Collodion removers due to contamination with Burkholderia ...

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

Fresh Location Announces Product Recall Due to Possible Listeria Contamination

January 8, 2020/in Recalls from FDA/by Heather Davis

Protein Snack Tray 6.44 oz total weight packaged in a 4-compartment plastic tray with UPC: 8-5511000804-6 and with Fresh by lot dates of: 12/21/19, 12/22/19, 12/24/19, 12/27/19, 12/28/19, 12/29/19, 12/31/19, 01/03/20, 01/04/20. Protein Trail Mix 3.52...

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

Mylan Initiates Voluntary Nationwide Recall of Three Lots of Nizatidine Capsules, USP, Due to the Detection of Trace Amounts of NDMA (N-Nitrosodimethylamine) Impurity Found in the Active Pharmaceutical Ingredient Manufactured by Solara Active Pharma Sciences Limited

January 8, 2020/in Recalls from FDA/by Heather Davis

Mylan N.V. (NASDAQ: MYL) today announced that its U.S. based Mylan Pharmaceuticals business is conducting a voluntary nationwide recall, to the consumer level, of three lots of Nizatidine Capsules, USP (including the 150mg and 300mg strengths). While M...

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

Appco Pharma LLC Issues Voluntary Nationwide Recall of Ranitidine Hydrochloride Capsules 150 mg and 300 mg Due to an Elevated Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA)

January 7, 2020/in Recalls from FDA/by Heather Davis

Appco Pharma LLC (Appco) is voluntarily recalling all quantities and lots, within expiry, of Ranitidine Hydrochloride Capsules to the Consumer level. Ranitidine Hydrochloride Capsules are being recalled because of the presence or potential presence of ...

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

Jeni’s Splendid Ice Creams Issues Voluntary Recall of Cold Brew with Coconut Cream

January 7, 2020/in Recalls from FDA/by Heather Davis

Jeni’s Splendid Ice Creams has initiated a voluntary recall of three batches of Cold Brew with Coconut Cream Non-Dairy Frozen Dessert pints because they may contain an undeclared milk allergen

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

About Heather Davis

Entries by Heather Davis

Taro Pharmaceuticals U.S.A., Inc. Issues Voluntary Nationwide Recall of Lamotrigine Tablets USP, 100 mg, 100 Count Bottles

Stryker Launches Voluntary Field Action for Specific Units of The LIFEPAK® 15 Monitor/Defibrillator

Libbey Glass Recalls Milk Bottles Due to Laceration Hazard

Thesaurus Global Marketing Recalls Tricycles Due to Violation of the Federal Lead Paint Ban; Risk of Poisoning; Sold Exclusively at Amazon.com (Recall Alert)

Boston Warehouse Trading Corp. Recalls Holiday Travel Mugs Due to Fire Hazard; Sold Exclusively at Meijer Stores

Mavidon Issues Voluntary Worldwide Recall of Manufactured Products Including Lemonprep® Tubes And Single Use Cups Pediaprep® Tubes And Single Use Cups Wave Prep® Tubes And Single Use Cups Cardio Prep Single Use Cups Due To Burkholderia Cepacia Contamination

Fresh Location Announces Product Recall Due to Possible Listeria Contamination

Mylan Initiates Voluntary Nationwide Recall of Three Lots of Nizatidine Capsules, USP, Due to the Detection of Trace Amounts of NDMA (N-Nitrosodimethylamine) Impurity Found in the Active Pharmaceutical Ingredient Manufactured by Solara Active Pharma Sciences Limited

Appco Pharma LLC Issues Voluntary Nationwide Recall of Ranitidine Hydrochloride Capsules 150 mg and 300 mg Due to an Elevated Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA)

Jeni’s Splendid Ice Creams Issues Voluntary Recall of Cold Brew with Coconut Cream

Contact Us

Amy Carter, Managing Shareholder

Heather Davis, Attorney

Latest Posts