Summary Company Announcement Date: October 21, 2021 FDA Publish Date: November 01, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description May contain small pieces of brown plastic Company Name: Ukrop’s Homestyle Foods Brand Name: Brand Name(s) Product Description: Product Description Green Salads and Chicken Caesar Wrap Company Announcement Recall Information Regarding…
Flowers Foods Issues Voluntary Recall on Certain Tastykake Multi-Pack Cupcakes Sold in Eight States Due to Possible Presence of Tiny Fragments of Metal Mesh Wire
Summary Company Announcement Date: October 31, 2021 FDA Publish Date: October 31, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential presence of tiny fragments of metal mesh wire Company Name: Flowers Foods, Inc. Brand Name: Brand Name(s) Product Description: Product Description Company Announcement As a precautionary measure, Flowers Foods, Inc….
Taylor Farms Mushroom Stir Fry, 9 Oz.
Summary Company Announcement Date: October 23, 2021 FDA Publish Date: October 23, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Listeria monocytogenes Company Name: Taylor Farms Brand Name: Brand Name(s) Taylor Farms Product Description: Product Description Mushroom Stir Fry Company Announcement Affects Kroger stores located in Georgia; South Carolina; Auburn, Alabama,…
Out of an Abundance of Caution Maryruth’s Announces Voluntary Recall of Two Lots of ITS Liquid Probiotic for Infants Because of the Potential for Contamination with Pseudomonas Aeruginosa
Summary Company Announcement Date: October 29, 2021 FDA Publish Date: October 29, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential contamination with Pseudomonas aeruginosa Company Name: MaryRuth’s Brand Name: Brand Name(s) MaryRuth’s Product Description: Product Description liquid probiotic for infants Company Announcement MaryRuth’s, a leading omni-channel health and wellness brand…
Zimmer Biomet Recalls ROSA One 3.1 Brain Application Due to Error in Software
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product ROSA One 3.1 Brain Application Product Codes and Lot Numbers: See Recall Database Entry Devices Recalled in the United States: 119 Distribution Date: December 1, 2019 to…
Former Naturopath Convicted of Trafficking in Misbranded Drugs He Claimed Could Treat and Prevent COVID
Department of JusticeU.S. Attorney’s OfficeWestern District of Washington FOR IMMEDIATE RELEASEMonday, October 25, 2021 Third federal conviction for Port Angeles Naturopath who lost his license in 2018 Tacoma – A former Port Angeles, Washington, naturopathic physician was convicted late last week of a federal felony related to his misbranding of products he claimed could prevent…
Florida Nurse Pleads Guilty to Tampering with Intensive Care Unit Patient’s Medication
Department of JusticeU.S. Attorney’s OfficeMiddle District of Florida FOR IMMEDIATE RELEASEThursday, October 28, 2021 Jacksonville, Florida – Jerome W. Clampitt II (42, Saint Johns) has pleaded guilty to tampering with a consumer product, specifically, injectable fentanyl. He faces a maximum penalty of 10 years in federal prison. A sentencing date has not yet been set….
Dole Fresh Vegetables Announces Precautionary Limited Recall of Garden Classic Salads for Possible Contamination with Listeria monocytogenes
Summary Company Announcement Date: October 29, 2021 FDA Publish Date: October 29, 2021 Product Type: Food & Beverages Produce Foodborne Illness Reason for Announcement: Recall Reason Description Potential contamination with Listeria monocytogenes Company Name: Dole Fresh Vegetables, Inc. Brand Name: Brand Name(s) Dole & others Product Description: Product Description garden salad Company Announcement Monterey, CA–October…
Datascope/Getinge/Maquet Recalls Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump Battery Packs Due to Risk of Battery Failure
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump Battery Packs Product Codes and Lot Numbers: See Recall Database Entry Devices Recalled in the United States: 137 battery packs Distribution Date:…
How Long Should You Take Certain Osteoporosis Drugs?
Reduce Your Risk A number of factors put both men and women at risk for osteoporosis, including age, race, family history, and a sedentary lifestyle. But there are also several ways you can reduce that risk, including: getting adequate amounts of calcium and Vitamin D through foods staying physically active, including weight-bearing exercise such as…