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 Imitation Crab and Shrimp Salad is being recalled because the contains statement does not declare pollock. 82 units are affected.
Arvis Hip & Knee 2.0 Instrument Sets are being recalled because the Impactor V-Block Assembly and Trackers may show early wear or corrosion on the exposed magnet face.
Albertsons store-made Cookies Cowboy 18 count is being recalled because the contains statement does not declare pecan. 982 units are affected.
The Large Volume Pump of the Ivenix Infusion System is being recalled because of the potential for the Cassette Loading Lever to break. 18,444 installed bases are affected.
Covidien EndoStitch Polysorb Single Use Loading Units are being recalled because holes in the pouch may compromise the sterile barrier. 2,448 units are affected.
CareOne Ultra Strength Calcium Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Albertsons store-made Shrimp & Surimi Ceviche Fresh is being recalled because the contains statement does not declare sea bream. 315 units are affected.
Albertsons store-made Brie & Bleu Cheese Tray Large is being recalled because the contains statement does not declare almond. Eight units are affected.
An Albertsons store-made cocktail tray is being recalled because the contains statement does not declare almond.
A Neptune Smart Docking Station is being recalled because it was not released from manufacturing and may not have completed required testing, leaving a potential shock risk.
Market Basket Antacid, calcium carbonate 1000 mg ultra strength, is being recalled because of the presence of small metallic particles in the chewable tablets.
Albertsons store-made Gourmet Dubai Cookie is being recalled because the contains statement does not declare pistachio.
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.
A further lot of Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, is being recalled because of small metallic particles in the chewable tablets.
The BD Pyxis MedStation 4000 medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Second Nature Keto Crunch Smart Mix is being recalled because the product may contain undeclared allergens, specifically cashews and pistachios, along with dried cherries.
The Andronico's Sweet Start Catering Tray Large, an Albertsons store-made item, is being recalled because the contains statement does not declare walnut. 14 units are affected.
H.E.B Extra Strength Calcium Carbonate Antacid Tablets, 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Pavilions Banana Nut Muffins single serve, an Albertsons store-made item, are being recalled because the contains statement does not declare walnut. 55 units are affected.
Albertsons store-made Kitchen Tray Sub Sandwich is being recalled because the contains statement does not declare pistachio. 13 units are affected.
Titanium/fluoroplastic piston stapes prostheses are being recalled because the device labeling states an incorrect functional length. Seven units are affected.
Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles.
CASE v7.0 Cardiac Testing Systems are being recalled because electrical sparking may occur at the printer head, and ignition of thermal paper could cause serious thermal injury.
Digital angiography and radiography systems are being recalled because contactors in the high voltage generator may weld together, leaving the power supply energized when the system is off.
Xyvona levorphanol tartrate tablets, 3 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.