Summary Company Announcement Date: June 23, 2021 FDA Publish Date: June 28, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared peanut protein Company Name: Bazzini LLC Brand Name: Brand Name(s) Trader Joe’s Product Description: Product Description Dark Chocolate Almond Butter Cups Company Announcement Bazzini LLC, Allentown, PA is, out of…
Stop Using Innova Medical Group SARS-CoV-2 Antigen Rapid Qualitative Test: FDA Safety Communication
Date Issued: June 10, 2021 The U.S. Food and Drug Administration (FDA) is warning the public to stop using the Innova Medical Group SARS-CoV-2 Antigen Rapid Qualitative Test for diagnostic use. The FDA has significant concerns that the performance of the test has not been adequately established, presenting a risk to health. In addition, labeling…
Perro bueno, alimento malo: alimentos para las personas que son malos para su perro
English Si considera al perro de la familia, pues, como de la familia—y no duda en arrojarle un trozo de su plato de vez en cuando, tenga cuidado. Algunos alimentos destinados para consumo humano pueden ser peligrosos, e incluso mortales, para su perro. ¿En qué sentido son las personas y los animales diferentes en lo…
Flexible Bronchoscopes and Updated Recommendations for Reprocessing: FDA Safety Communication
Date Issued: June 25, 2021 The U.S. Food and Drug Administration (FDA) is providing updated information about medical device adverse event reports and recommendations for health care providers on bronchoscopes. This is a supplement to the 2015 safety communication on reprocessed flexible bronchoscopes. Recommendations for Patients and Caregivers The recommendations have not changed from the…
Smiths Medical Recalls Jelco Hypodermic Needle-Pro Fixed Needle Insulin Syringes for Skewed Graduated Marks on Syringe Barrel That May Cause Insulin Overdose or Underdose
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 Jelco Hypodermic Needle-Pro Fixed Needle Insulin Syringes Models and Lot Model Number Name Lot Number 4428-1 Jelco Hypodermic Needle-Pro Fixed Needle Insulin Syringe 28Gx1/2” 1CC 4046543, 4062235…
Avid Medical Recalls Medical Convenience Kits for Risk of Fungal Contamination
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 Adult Chest Tube Tray Fistula On-Off Kit Fistula (On/Off All in One bag) Dialysis Access Part and Lot Numbers: See “Full List of Affected Devices” Distribution Dates:…
New Hampshire Man Pleads Guilty to Tampering With a Consumer Product
Department of JusticeU.S. Attorney’s OfficeDistrict of Maine FOR IMMEDIATE RELEASEThursday, June 24, 2021 PORTLAND, Maine: A Dover, New Hampshire man pleaded guilty today in federal court to one count of tampering with a consumer product, Acting U.S. Attorney Donald E. Clark announced. According to court records, Nicholas Mitchell, 39, was an employee of a Maine…
Dole Diversified North America, Inc. Announces Limited Recall of Dole™ Fresh Blueberries for Potential Cyclospora Contamination
Summary Company Announcement Date: June 24, 2021 FDA Publish Date: June 25, 2021 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Cyclospora contamination Company Name: Dole Diversified North America, Inc. Brand Name: Brand Name(s) Product Description: Product Description Fresh Blueberries FDA Announcement Dole Diversified North America, Inc. is recalling a limited number…
Avanti Frozen Foods Recalls Frozen Cooked Shrimp Because of Possible Health Risk
Summary Company Announcement Date: June 25, 2021 FDA Publish Date: June 25, 2021 Product Type: Food & Beverages Shellfish Foodborne Illness Reason for Announcement: Recall Reason Description Salmonella Company Name: Avanti Frozen Foods Pvt. Ltd Brand Name: Brand Name(s) Censea, Hannaford, Open acres, Honest catch, COS and others Product Description: Product Description Frozen shrimp, cooked,…
DeRoyal Industries Recalls Surgical Procedure Packs for Mislabeled Lidocaine
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 DeRoyal Pacemaker Tray Pgybk Lot Number 54239375, exp. 02/01/2022 DeRoyal Heart Cath Procedure Pack Lot Numbers: 54310362, exp. 01/01/2022; 54366825, exp. 01/01/2022 DeRoyal Angio Cath Removal Tray…