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Urgent – Food Recall Because of Potential Undeclared Allergen Due to Mislabel
As a precautionary measure, Seneca Foods Corporation is announcing a voluntary recall of mislabeled Hy-Vee Turkey gravy in glass jars that actually contains beef gravy. This product could potentially contain a soy allergen which is not declared on the label. Seneca is now retrieving improperly lab (Source: FDA Food Alergies)
Source: FDA Food Alergies - November 21, 2023 Category: Food Science Authors: FDA Source Type: alerts

Datascope Corp. - SENSATION PLUS 7.5Fr IAB - Class 2 Recall
SENSATION PLUS 7.5Fr IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description Part Number SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES D684-00-0568-01 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (W/O STATLOCK) D684-00-0568-03 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (WITH PRESSURE D684-00-0568-05 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES (TURKEY) D684-00-0568-09 SENSATION PLUS 7.5Fr. 40cc WITH ACCESSORIES, US ONLY D684-00-0568-01U PACKAGED INSERTION KIT - SENSATION PLUS 7.5 Fr. 40 cc IAB D884-00-0019-22 (...
Source: Medical Device Recalls - July 22, 2023 Category: Medical Devices Source Type: alerts

Datascope Corp. - LINEAR 7.5Fr.IAB - Class 2 Recall
LINEAR 7.5Fr.IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description Part Number LINEAR 7.5Fr. 34cc IAB WITH ACCESSORIES D684-00-0479-01 LINEAR 7.5Fr. 34cc IAB WITH ACCESSORIES (APA) D684-00-0479-02 LINEAR 7.5Fr. 34cc IAB WITH ACCESSORIES (CHINA) D684-00-0479-01C LINEAR 7.5Fr. 34cc IAB WITH ACCESSORIES (APA)(CHINA) D684-00-0479-02C LINEAR 7.5Fr. 34cc IAB WITH ACCESSORIES (INDIA) D684-00-0479-07 LINEAR 7.5Fr. 34cc IAB WITH ACCESSORIES (APA) (INDIA) D684-00-0479-08 LINEAR 7.5Fr. 34cc IAB WITH ACCESSORIES (TURK...
Source: Medical Device Recalls - July 22, 2023 Category: Medical Devices Source Type: alerts

Datascope Corp. - MEGA 8Fr. IAB - Class 2 Recall
MEGA 8Fr. IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description Part Number MEGA 8Fr. 50cc IAB WITH STATLOCK D684-00-0296-01 MEGA 8Fr. 50cc IAB WITH STATLOCK & APA D684-00-0296-02 MEGA 8Fr. 50cc IAB WITH ACCESSORIES (W/O STATLOCK) D684-00-0296-03 MEGA 8Fr. 50cc IAB WITH ACCESSORIES (TURKEY) D684-00-0296-09 MEGA 8Fr. 50cc IAB WITH ACCESSORIES WITH APA (TURKEY) D684-00-0296-10 MEGA 8Fr. 50cc IAB WITH ACCESSORIES, US ONLY D684-00-0296-01U MEGA 8Fr. 50cc IAB WITH ACCESSORIES, (APA) US ONLY D684-00-0296-02U...
Source: Medical Device Recalls - July 22, 2023 Category: Medical Devices Source Type: alerts

Datascope Corp. - SENSATION IAB - Class 2 Recall
SENSATION 7 Fr. IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description Part Number SENSATION 7 Fr. 34cc IAB WITH ACCESSORIES (CHINA) D684-00-0469-01C SENSATION 7 Fr. 34cc IAB WITH ACCESSORIES (INDIA) D684-00-0469-07 SENSATION 7 Fr. 40cc IAB WITH ACCESSORIES (CHINA) D684-00-0470-01C SENSATION 7 Fr. 40cc IAB WITH ACCESSORIES (INDIA) D684-00-0470-07 SENSATION 7 Fr. 40cc IAB WITH ACCESSORIES (TURKEY) D684-00-0470-09 SENSATION 7 Fr. 40cc IAB WITH ACCESSORIES D684-00-0470-01 SENSATION 7 Fr. 40cc IAB W...
Source: Medical Device Recalls - July 22, 2023 Category: Medical Devices Source Type: alerts

Datascope Corp. - MEGA 7.5Fr.IAB - Class 2 Recall
MEGA 7.5Fr.IAB , Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description Part Number MEGA 7.5Fr. 40cc IAB WITH ACCESSORIES D684-00-0295-01 MEGA 7.5Fr. 40cc IAB WITH ACCESSORIES (APA) D684-00-0295-02 MEGA 7.5Fr. 40cc IAB WITH ACCESSORIES (W/O STATLOCK) D684-00-0295-03 MEGA 7.5Fr. 40cc IAB WITH ACCESSORIES (CHINA) D684-00-0295-05 MEGA 7.5Fr. 40cc IAB WITH ACCESSORIES AND APA (CHINA) D684-00-0295-06 MEGA 7.5Fr. 40cc IAB WITH ACCESSORIES ...
Source: Medical Device Recalls - July 22, 2023 Category: Medical Devices Source Type: alerts

Datascope Corp. - SENSATION PLUS 8Fr. IAB - Class 2 Recall
SENSATION PLUS 8Fr. IAB, Intra-Aortic Balloon Catheter and Accessories, used to provide counter pulsation therapy in the aorta Product Description Part Number SENSATION PLUS 8Fr. 50cc IAB WITH ACCESSORIES D684-00-0576-01 SENSATION PLUS 8Fr. 50cc IAB WITH ACCESSORIES (WITH PRESSURE D684-00-0576-03 SENSATION PLUS 8Fr. 50cc IAB WITH ACCESSORIES (WITH PRESSURE D684-00-0576-05 SENSATION PLUS 8Fr. 50cc IAB WITH ACCESSORIES (TURKEY) D684-00-0576-09 SENSATION PLUS 8Fr. 50cc IAB WITH ACCESSORIES, US ONLY D684-00-0576-01U PACKAGED INSERTION KIT - SENSATION PLUS 8 Fr. 50 cc IAB D884-00-00...
Source: Medical Device Recalls - July 22, 2023 Category: Medical Devices Source Type: alerts

GHGA, LLC. Issues Allergy Alert for Undeclared Sesame in Turkey and Havarti Sandwich
GHGA, LLC. is voluntarily recalling 8.55 oz packages of Turkey and Havarti Sandwiches due to undeclared sesame in bread. People who are allergic to sesame run the risk of serious or life-threatening allergic reaction if they consume this product. The recalled product was shipped to Kroger stores in (Source: FDA Food Safety)
Source: FDA Food Safety - April 27, 2023 Category: Food Science Authors: FDA Source Type: alerts

GH Foods CA, LLC. Issues Allergy Alert for Undeclared Sesame in Turkey and Havarti Sandwich
GH Foods CA, LLC. is voluntarily recalling 8.55 oz packages of Turkey and Havarti Sandwiches due to undeclared sesame in bread. People who are allergic to sesame run the risk of serious or life-threatening allergic reaction if they consume this product. (Source: FDA Food Alergies)
Source: FDA Food Alergies - April 26, 2023 Category: Food Science Authors: FDA Source Type: alerts

GHSW, LLC. Issues Allergy Alert for Undeclared Sesame in Turkey and Havarti Sandwich
GHSW, LLC. is voluntarily recalling 8.55 oz packages of Turkey and Havarti Sandwiches due to undeclared sesame in bread. People who are allergic to sesame run the risk of serious or life-threatening allergic reaction if they consume this product. The recalled product was shipped to Dillon stores in (Source: FDA Food Safety)
Source: FDA Food Safety - April 26, 2023 Category: Food Science Authors: FDA Source Type: alerts

A-20 (beef, pork, lamb, chicken, and turkey) solution [DNA Labs, Inc.]
Updated Date: Mon, 30 May 2022 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 30, 2022 Category: Drugs & Pharmacology Source Type: alerts

Heartware, Inc. - HeartWare Ventricular Assist Device (HVAD) System - Class 2 Recall
HeartWare Ventricular Assist Device (HVAD) System, individual pamphlets: HVAD¿ System Emergency Responder Guide (FI-Finnish) HVAD¿ System Emergency Responder Guide (FI-Finnish) HVAD¿ System Emergency Responder Guide (FI-Finnish) HVAD¿ System Emergency Responder Guide (FI-Finnish) HVAD¿ System Instructions For Use (FI) HVAD¿ System Instructions For Use (FI) HVAD¿ System Patient Manual (FI-Finnish) HVAD¿ System Patient Manual (FI-Finnish) HVAD¿ System Patient Manual (FI-Finnish) HVAD¿ System Patient Manual (FI-Finnish) HVAD¿ System Patient Manual (FI-Finnish) HVAD¿...
Source: Medical Device Recalls - May 18, 2022 Category: Medical Devices Source Type: alerts

Turkey Hill Dairy Issues Voluntary Recall and Allergy Alert for Undeclared Peanut in Select Chocolate Marshmallow Premium Ice Cream Containers
Turkey Hill Dairy of Conestoga, Pa., is recalling select 48 oz containers of its Chocolate Marshmallow Premium Ice Cream because the product may contain undeclared peanuts. People who have an allergy to peanuts run the risk of serious or life-threatening allergic reaction if they consume these produ (Source: FDA Food Alergies)
Source: FDA Food Alergies - April 21, 2022 Category: Food Science Authors: FDA Source Type: alerts