Insulet Corporation - Insulet Omnipod DASH Insulin Management System - Class 2 Recall
Omnipod DASH Insulin Management System User Guide (OUS Only) Product Catalog Number: PT 000002 XXX XXX XX PT 000318 PT 000319 Distributed to: Canada (French only), the Netherlands, France, Austria, Germany, Belgium, Greece, Turkey, Norway, Sweden, Denmark, and Finland (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 11, 2021 Category: Medical Devices Source Type: alerts
SPATHERAPY ANTIBACTERIAL FRENCH LAVENDER (alcohol) gel [Shalom International Corp]
Updated Date: Thu, 28 Jan 2021 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - January 28, 2021 Category: Drugs & Pharmacology Source Type: alerts
Door County Coffee & Tea Co Issues Allergy Alert on Undeclared Milk and Soy in French Vanilla Flavored Cappuccino Single Serve Cups
Door County Coffee& Tea Co of Sturgeon Bay, WI, is recalling its 5.1 ounce packages of French Vanilla Flavored Cappuccino Single Serve Cups because they may contain undeclared Milk and Soy. People who have allergies to Milk and Soy run the risk of serious or life-threatening allergic reaction if th (Source: FDA Food Safety)
Source: FDA Food Safety - January 21, 2021 Category: Food Science Authors: FDA Source Type: alerts
Door County Coffee & Tea Co. Issues Allergy Alert on Undeclared Milk and Soy in French Vanilla Flavored Cappuccino Single Serve Cups
Door County Coffee& Tea Co of Sturgeon Bay, WI, is recalling its 5.1 ounce packages of French Vanilla Flavored Cappuccino Single Serve Cups because they may contain undeclared Milk and Soy. People who have allergies to Milk and Soy run the risk of serious or life-threatening allergic reaction if th (Source: FDA Food Alergies)
Source: FDA Food Alergies - January 21, 2021 Category: Food Science Authors: FDA Source Type: alerts
Medline Industries Inc - Medline Greffe AorteLF - Class 2 Recall
Greffe Aorte-LF (product info is in French); Model DYNJ31877F - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 8, 2021 Category: Medical Devices Source Type: alerts
Legendary Baking Issues Allergy Alert for Potential Undeclared Pecan in Product Labeled as French Silk Pie
Legendary Baking of Chaska, MN is voluntarily recalling a single lot of item number 7545 - French Silk Pie. This product is being recalled due to a potential undeclared pecan allergen. People who have an allergy or severe sensitivity to pecans run the risk of serious or life threatening allergic rea (Source: FDA Food Safety)
Source: FDA Food Safety - December 24, 2020 Category: Food Science Authors: FDA Source Type: alerts
LUSTER PREMIUM WHITE PRO SONIC DENTAL WHITENING SYSTEM (sodium monofluorophosphate) kit [French Transit, Ltd.]
Updated Date: Fri, 18 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 18, 2020 Category: Drugs & Pharmacology Source Type: alerts
LUSTER PREMIUM WHITE NOW (sodium fluoride) paste [French Transit, Ltd.]
Updated Date: Fri, 18 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 18, 2020 Category: Drugs & Pharmacology Source Type: alerts
LUSTER PREMIUM WHITE AM/PM (sodium fluoride and sodium monofluorophosphate) kit [French Transit, Ltd.]
Updated Date: Fri, 18 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 18, 2020 Category: Drugs & Pharmacology Source Type: alerts
LUSTER PREMIUM WHITE PRO LIGHT DENTAL WHITENING SYSTEM (sodium monofluorophosphate) kit [French Transit, Ltd.]
Updated Date: Fri, 18 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 18, 2020 Category: Drugs & Pharmacology Source Type: alerts
LUSTER PREMIUM WHITE POWER WHITE PRO (sodium monofluorophosphate) paste [French Transit, Ltd.]
Updated Date: Fri, 18 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 18, 2020 Category: Drugs & Pharmacology Source Type: alerts
AROMA GURU ANTIBACTERIAL FRENCH LAVENDER (hand soap) liquid [GURUNANDA LLC]
Updated Date: Fri, 04 Dec 2020 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 4, 2020 Category: Drugs & Pharmacology Source Type: alerts
Dole Fresh Vegetables Announces Limited Recall of Organic Romaine Hearts
Dole Fresh Vegetables, Inc. is voluntarily recalling a limited number of cases of organic romaine hearts. The products being recalled are Dole ™ Organic Romaine Hearts 3pk (UPC 0-71430-90061-1), combined English/French packaging, with Harvested-On dates of 10-23-20 and 10-26-20, and Wild Harvest Orga (Source: FDA Food Safety)
Source: FDA Food Safety - November 21, 2020 Category: Food Science Authors: FDA Source Type: alerts
Cook Inc. - Percutaneous Neonatal Pigtail Nephrostomy Set and Pediatric Nephrostomy Stent Set - Class 2 Recall
Percutaneous Neonatal Pigtail Nephrostomy Set, Reference Part Number 080106, Order Number G14508. The set contains a 22 gage, 5 cm Chiba Needle; an 18 gage, 5 cm trocar needle; an .038-inch (.97 mm) diameter, 30 cm PTFE-coated stainless steel; a 5, 6, and 7 French, 10 cm radiopaque dilator; a 6 French, 7 cm radiopaque pigtail catheter; a retention disc with pull tie; and a 10 French, 10 cm clear, polyvinylchloride connecting tube with one-way stopcock. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 15, 2020 Category: Medical Devices Source Type: alerts
Cook Inc. - Percutaneous Neonatal Pigtail Nephrostomy Set and Pediatric Nephrostomy Stent Set - Class 2 Recall
Pediatric Nephrostomy Stent Set, Reference Part Numbers 080208-S6 and 080208-S7, Order Numbers G15034 and G15035. The set contains a radiopaque pigtail catheter and stent, retention disc with pull tie, and a 10 French, 30 cm polyvinylchloride connecting tube with one-way stopcock. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 15, 2020 Category: Medical Devices Source Type: alerts
