State
72,907 recalls have nationwide distribution and so reach North Dakota. 2,921 additional recalls listed North Dakota specifically in their distribution scope.
Of the 2,921 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 727 (25%) are Severe.
Which agencies issued them
These figures cover only the 2,921 recalls whose distribution notice names North Dakota specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Albertsons store-made Platter Loaf Sliced, 20 count, is being recalled because the contains statement does not declare walnut. 20 units are affected.
The BD Pyxis Anesthesia Station 4000 is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, are being recalled after failing dissolution specifications, with olmesartan medoxomil content below specification.
Second Nature Keto Crunch Smart Mix is being recalled because the product may contain undeclared allergens, specifically cashews and pistachios, along with dried cherries.
BD Pyxis MedStation ES Tower medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Albertsons store-made Cookies Cowboy 18 count is being recalled because the contains statement does not declare pecan. 982 units are affected.
Albertsons store-made seafood salad is being recalled because the contains statement does not declare crab. 114 units are affected.
Albertsons store-made Kitchen Caesar Salads in large and small sizes are being recalled because the contains statement does not declare anchovy. 39 units are affected.
Albertsons store-made Pie Peach Melba 9-inch is being recalled because the contains statement does not declare almond. Seven units are affected.
Equaline Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.
Exacta Mix Vented Micro-Volume Inlet tubing sets are being recalled because affected lots may contain 0.8-micron filters in place of the validated 3-micron filters.
Albertsons store-made Wok Pad Thai Chicken with Egg Roll is being recalled because the contains statement does not declare anchovy. 12 units are affected.
Albertsons store-made Platter Pastry Mini Breakfast, 28 count, is being recalled because the contains statement does not declare almond. 75 units are affected.
Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Philips Azurion 7M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
BD Pyxis Mini Main medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 709 units affected.
Albertsons store-made pork meat pies are being recalled because the contains statement does not declare anchovy. 790 units in total are affected.
Albertsons store-made Banana Nut Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 434 units are affected.
Albertsons store-made Platter Catering Loaf Cake Slice is being recalled because the contains statement does not declare walnut. 92 units are affected.
Philips Azurion 5M20 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Philips Azurion 7B12/12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Arvis Hip & Knee 3.0 Instrument Sets are being recalled because the V-Block Assembly and Trackers A, B, C and E may show early wear or corrosion on the exposed magnet face.
Albertsons store-made Cake Raspberry Moon 8-inch 2-layer is being recalled because the contains statement does not declare almond. 25 units are affected.
The BD Pyxis MedStation ES medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.