Sammy ’s Milk Providing a Warning Against the Use of Goat Milk Toddler Formula as Infant Formula
Newport Beach, California - Sammy's Milk, a local company, has been asked by the Food and Drug Administration (FDA) to provide a warning against the use of its Goat Milk Toddler Formula as an infant formula because the FDA is concerned that the formula may not meet all FDA requirements for infant fo (Source: FDA Food Safety)
Source: FDA Food Safety - April 19, 2024 Category: Food Science Authors: FDA Source Type: alerts
Consumer Protection Issues Food Safety Warning for EZ Noble Sushi EZ Noble Sushi is voluntarily recalling the products, which contained unlabeled allergens
— The Connecticut Department of Consumer Protection Food, Standards and Product Safety division is urging Connecticut residents to check their refrigerators for EZ Noble Sushi, which was available for purchase this week at Geissler’s Supermarkets in Connecticut and Massachusetts. East Windsor-ba sed (Source: FDA Food Safety)
Source: FDA Food Safety - August 11, 2022 Category: Food Science Authors: FDA Source Type: alerts
Tova Industries; LLC. Issues Allergy Alert on Undeclared Milk in Carbquik Mug Cake Double Chocolate Chunk OU-Dairy
Tova Industries; LLC of Louisville, KY is voluntarily recalling Carbquik Mug Cake Double Chocolate Chunk OU-Dairy (Water and Butter Prep), because it contains an undeclared milk allergen in the allergen warning statement. A limited amount, approximately 1700 retail packs, of Carbquik Mug Cake Double (Source: FDA Food Safety)
Source: FDA Food Safety - April 1, 2022 Category: Food Science Authors: FDA Source Type: alerts
Beckman Coulter Inc. - Unsaturated Iron Binding Capacity - Class 2 Recall
UIBC; Catalog Number: OSR61205; UDI (01) 15099590011925; IVD; Rx Only; WARNING H316 H317 H351 H373 H411 - Product Usage: System reagent for the quantitative determination of Unsaturated Iron Binding Capacity (UIBC) in human serum and plasma on Beckman Coulter AU analyzers. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 1, 2020 Category: Medical Devices Source Type: alerts
Hail Merry Issues Voluntary Recall Due to Labeling Error
Hail Merry LLC, a plant-based snack food company, voluntarily recalls its Meyer Lemon Mini Miracle Tart Party Pack of 6 from the market due to a labeling error. The products contain cashews as listed on the "Ingredients" label, however the "Contains" allergen warning statement does not specifically identify "cashews." (Source: FDA Food Alergies)
Source: FDA Food Alergies - August 27, 2019 Category: Food Science Authors: FDA Source Type: alerts
U.S Trading Recalls RATTAN SHOOTS in BRINE Due to Undeclared Sulfites
US TRADING COMPANY is warning consumers not to consume GLOBAL PRIDE RATTAN SHOOT IN BRINE. The product is being recalled because the product contains Sulfites which is not declared on the labeling. (Source: FDA Food Alergies)
Source: FDA Food Alergies - May 18, 2019 Category: Food Science Authors: FDA Source Type: alerts
FDA: Gout Drug Raises Death Risk
(MedPage Today) -- Black box warning, second-line use being required (Source: MedPage Today Product Alert)
Source: MedPage Today Product Alert - February 21, 2019 Category: Drugs & Pharmacology Source Type: alerts
CareFusion 303, Inc. - Infusion Set Alaris Pump Module/Medley Pump Module/Gemini Infusion Pump - Class 2 Recall
Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris Pump Module/Medley Pump Module/Gemini Infusion Pump, REF 10011301, CareFusion, WARNING: TO PREVENT FREE-FLOW, CLOSE SET CLAMP WHEN SAFETY CLAMP FITMENT ON PUMP SEGMENT IS OPEN, Fluid path is STERILE and NONPYROGENIC. 12276678 Rev 00 -VersaSafe Infusion Set Alaris Pump Module/Medley Pump Module/Gemini Infusion Pump, REF 2120-0500, WARNING: TO PREVENT FREE-FLOW, CLOSE SET CLAMP WHEN SAFETY CLAMP ON PUMP SEGMENT IS OPEN. FLUID PATH IS STERILE and NON-PYROGENIC. PRODUCT is sterilized by GAMMA IRRADIATION. CareFusion, 630-01104 Rev 00 -SmartSite Infusio...
Source: Medical Device Recalls - November 5, 2018 Category: Medical Devices Source Type: alerts
FDA Warns on OTC Teething Products with Benzocaine
(MedPage Today) -- Asks manufacturers to pull products, will require warnings (Source: MedPage Today Product Alert)
Source: MedPage Today Product Alert - May 23, 2018 Category: Drugs & Pharmacology Source Type: alerts
Boston Scientific Corporation - AngioJet Ultra 5000 A Console: - Class 2 Recall
AngioJet¿ Ultra 5000 A Console:Foot Switch Material number (U PN) 105650 Cardiovascular: The Console is a multiple-use device that controls the Thrombectomy Set. It drives the pump, regulates fluid inflow and outflow, provides the operator with Ultra System set-up prompts, total infused saline volume, and Ultra System malfunction warnings. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 4, 2017 Category: Medical Equipment Source Type: alerts
Fluoroquinolone Antibacterial Drugs for Systemic Use: Drug Safety Communication - Warnings Updated Due to Disabling Side Effects
Use associated with disabling and potentially permanent side effects of the tendons, muscles, joints, nerves, and central nervous system that can occur together in the same patient. (Source: FDA MedWatch Safety Alert)
Source: FDA MedWatch Safety Alert - July 26, 2016 Category: American Health Source Type: alerts
Medtronic Navigation - Medtronic PoleStar Intraoperative MRI system (N20 / N30) - Class 2 Recall
PoleStar system (N20 / N30) Warning Lamps Control Box, Warning Lamps Control Box Cables, Thermoflex Chiller Product The PoleStar Surgical MRI System is intended for use as an intraoperative imaging device to produce MRI images of sections of the head selected by the physician. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 7, 2016 Category: Medical Equipment Source Type: alerts
Caprelsa (vandetanib)
Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER)
July 2016
WARNINGS AND PRECAUTIONS
Severe Skin Reactions (previously Skin Reactions and Stevens-Johnson Syndrome)
Severe and... (Source: Drugs.com - Labeling Changes)
Source: Drugs.com - Labeling Changes - July 1, 2016 Category: Drugs & Pharmacology Source Type: alerts
Avelox (moxifloxacin hydrochloride)
Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER)
July 2016
BOX WARNING (revised)
WARNING: SERIOUS ADVERSE REACTIONS INCLUDING TENDINITIS, TENDON RUPTURE, PERIPHERAL NEUROPATHY,... (Source: Drugs.com - Labeling Changes)
Source: Drugs.com - Labeling Changes - July 1, 2016 Category: Drugs & Pharmacology Source Type: alerts
Cipro (ciprofloxacin hydrochloride) Tablets, Solution, Oral SuspensionCipro XR (ciprofloxacin extended release) Tablets
Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER)
July 2016
BOX WARNING (revised)
WARNING: SERIOUS ADVERSE REACTIONS INCLUDING TENDINITIS, TENDON RUPTURE, PERIPHERAL NEUROPATHY,... (Source: Drugs.com - Labeling Changes)
Source: Drugs.com - Labeling Changes - July 1, 2016 Category: Drugs & Pharmacology Source Type: alerts
