This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. The affected…
Gas Powered Emergency Resuscitator Recall: Mercury Medical Removes Neo-Tee T-Piece Resuscitator Due to An Undersized Spring in The Controller That May Prevent the Device from Delivering the Required Pressure Levels Needed for Effective Ventilation
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product What to Do On December 5, 2024, Mercury Medical sent all affected customers an Urgent…
Pressure Monitoring Device Recall: Medtronic Neurosurgery Issues Correction for Becker and Exacta External Drainage and Monitoring Systems Due to Cracks And/Or Leaks in Stopcocks
This recall involves correcting certain devices, and does not involve removing them from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it without correction. Affected Product Product Names: Becker External Drainage and Monitoring…
Update on Alert: Nephroscope Sheath Issue from Trokamed GmbH
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. This recall involves updating instructions for using certain devices, and does not involve removing them from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or…
Update on Alert: Fluid Delivery Set Issue from Medline
99000069 FDS, 135, CHMN, W/F, MLL, RC(2), PG 0000128741 10193489069587 30193489069581 99000069 FDS, 135, CHMN, W/F, MLL, RC(2), PG 0000134505 10193489069587 30193489069581 99000069 FDS, 135, CHMN, W/F, MLL, RC(2), PG 0000133893 10193489069587 30193489069581 99000069 FDS, 135, CHMN, W/F, MLL, RC(2), PG 0000135769 10193489069587 30193489069581 99000069 FDS, 135, CHMN, W/F, MLL, RC(2), PG 0000139596 10193489069587 30193489069581…
Update on Alert: Extracorporeal Blood Circuit Issue from Nuwellis
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. The affected…
Blue Ridge Beef Issues a Recall of Blue Ridge Beef Natural Mix Due to Salmonella Contamination
Summary Company Announcement Date: January 31, 2025 FDA Publish Date: January 31, 2025 Product Type: Animal & VeterinaryFood & Beverages Pet Food Foodborne Illness Reason for Announcement: Recall Reason Description Salmonella contamination Company Name: Blue Ridge Beef Brand Name: Brand Name(s) Blue Ridge Beef Product Description: Product Description Natural Mix Company Announcement STATESVILLE, NC –…
Gerber Products Company Announces Recall and Discontinuation of All Batches of Gerber® Soothe N Chew® Teething Sticks Due To Choking Hazard
Summary Company Announcement Date: January 31, 2025 FDA Publish Date: January 31, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential choking hazard for babies and young children Company Name: Gerber Products Company Brand Name: Brand Name(s) Product Description: Product Description Gerber® Soothe N Chew® Teething Sticks Company Announcement…
Olympus Issues Medical Device Advisory Notice to Use Alternative Devices to the MAJ-891 Forceps/Irrigation Plug
Summary Company Announcement Date: January 29, 2025 FDA Publish Date: January 30, 2025 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Risk of device contamination that may result from improper reprocessing. Company Name: Olympus Corporation Brand Name: Brand Name(s) Product Description: Product Description MAJ-891 endoscope accessory Company Announcement CENTER VALLEY, Pa., (January 29,…
United Natural Trading LLC Announces Allergy Alert for Undeclared Milk in Fresh Direct Dark Chocolate Covered Pretzels
Summary Company Announcement Date: January 30, 2025 FDA Publish Date: January 30, 2025 Product Type: Food & Beverages Snack Food Item Allergens Reason for Announcement: Recall Reason Description Undeclared milk Company Name: United Natural Trading LLC Brand Name: Brand Name(s) Fresh Direct Product Description: Product Description Dark Chocolate Covered Pretzels Company Announcement FOR IMMEDIATE RELEASE…