Ascom Telligence Nurse Call System recall — FDA Z-0486-2019
There is an issue that could cause the Telligence System Gateway II, NGGTWY2 H, to stop communicating to the hallway devices connected to it. When this occurs, the dome lights connected to…
Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
There is an issue that could cause the Telligence System Gateway II, NGGTWY2 H, to stop communicating to the hallway devices connected to it. When this occurs, the dome lights connected to…
Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in a redundant fashion to make the interlock system single-fault tolerant.
BD Vacutainer Urine Collection Cups may contribute to a slight elevation of Red Blood Cell (RBC) counts when used with the Sysmex UF Series Analyzers. BD recommends following Good Clinical…
Potential electric leakage affecting the user.
A manufacturing defect on the amplifier board of the Flow Cytometers my cause signal loss and/or signal drifting resulting in absence of data or a population shift in the data plots. This…
BD Vacutainer Urine Collection Cups may contribute to a slight elevation of Red Blood Cell (RBC) counts when used with the Sysmex UF Series Analyzers. BD recommends following Good Clinical…
Potential electric leakage affecting the user.
A safety problem with installation and maintenance could lead to the breakage of the two steel cables that support the equipment to its roof anchor. Due to this, the equipment may fall and…
The firm identified an issue with the basal calculator identified on the Android version of the Insulia application. The bug could lead from low-impact to high-impact hypoglycemia depending…
The firm noticed that multiple snack food items for a customer had the same information panel. Therefore the ingredient list and allergen information is incorrect.
The product tested positive for Salmonella.
Buttered popcorn contains a milk ingredient (butter), but fails to declare milk on the label.
Recall of products manufactured with vegetables from McCain Foods USA and currently under recall for potential Salmonella and/or Listeria Monocytogenes contamination
Recall of products manufactured with vegetables from McCain Foods USA and currently under recall for potential Salmonella and/or Listeria Monocytogenes contamination
The firm noticed that multiple snack food items for a customer had the same information panel. Therefore the ingredient list and allergen information is incorrect.
The product tested positive for Salmonella.
Cranberry Walnut Salad contains the incorrect ingredient statement on the bottom of the container and does not declare wheat or walnuts.
Products recalled due to potential contamination with Listeria monocytogenes or Salmonella.
The product tested positive for Salmonella.
The firm noticed that multiple snack food items for a customer had the same information panel. Therefore the ingredient list and allergen information is incorrect.
FDA analysis of Dairy Free Dark Chocolate found high levels of milk protein in the chocolate bars
Customer complaint of ingredient listed in name of product (Quinoa) but product contained Farro and not quinoa. Farro is declared as an ingredient but wheat is undeclared on the label.
FDA analysis of Dairy Free Dark Chocolate found high levels of milk protein in the chocolate bars.
The firm noticed that multiple snack food items for a customer had the same information panel. Therefore the ingredient list and allergen information is incorrect.
Browse recent months with enough recall history for useful comparison.