State
72,907 recalls have nationwide distribution and so reach Idaho. 3,517 additional recalls listed Idaho specifically in their distribution scope.
Of the 3,517 recalls naming Idaho we have scored against our rubric, 364 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,023 (29%) are Severe.
Which agencies issued them
These figures cover only the 3,517 recalls whose distribution notice names Idaho 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 Twisted Bliss Pretzel Tray is being recalled because the contains statement does not declare almond. Two units are affected.
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.
Titanium/fluoroplastic piston stapes prostheses are being recalled because the device labeling states an incorrect functional length. Seven units 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.
Lannett Niacin Extended-release Tablets, 1,000 mg, are being recalled after a stability test returned an out-of-specification low result for Stage 3 dissolution at 24 hours.
Albertsons store-made Cake Pav Chocolate Lady Madeleines Strawberry is being recalled because the contains statement does not declare almond. Six units are affected.
24/7 life by 7-Eleven Extra Strength Antacid Tablets, calcium carbonate 750 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.
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 pork meat pies are being recalled because the contains statement does not declare anchovy. 790 units in total are affected.
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.
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.
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.
Philips Azurion 7M20 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.
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.
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.
Haleon Tums Antacid Assorted Fruit Tablets, 750 mg, in 330-count bottles are being recalled because of the presence of small metallic particles in the chewable tablets.
Albertsons store-made Platter Cheeses of France is being recalled because the contains statement does not declare almond. 31 units 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 Mexican Wedding Cookies, 8 count, are being recalled because the contains statement does not declare pecan. 445 units are affected.
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.
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.
Philips Azurion 7B20/15 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable. 156 units affected.
Philips Azurion 3M12 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 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.