State
72,913 recalls have nationwide distribution and so reach Arizona. 8,381 additional recalls listed Arizona specifically in their distribution scope.
Of the 8,381 recalls naming Arizona we have scored against our rubric, 1,313 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,717 (20%) are Severe.
Which agencies issued them
These figures cover only the 8,381 recalls whose distribution notice names Arizona specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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.
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.
Albertsons store-made Ready Meals Duo Seafood Salad with Crackers is being recalled because the contains statement does not declare whiting. 286 units are affected.
Duloxetine DR Capsules, 30 mg, relabeled by Enovachem are being recalled over CGMP deviations and N-nitroso-duloxetine above the FDA acceptable intake limit.
Albertsons store-made Kitchen Salad Turkey Poppyseed is being recalled because the contains statement does not declare almond.
Albertsons store-made Oatmeal Raisin Cookies, 10 count, are being recalled because the contains statement does not declare almond. 62 units are affected.
Albertsons store-made Ready Meals Meatloaf is being recalled because the contains statement does not declare anchovy. 353 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.
Hy-Vee Ultra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Philips Azurion 5M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may produce a dark image that is not clinically usable.
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.
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.
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.
Straus Family Creamery Organic Super Premium Strawberry Ice Cream in quart and pint sizes is being recalled over potential contamination with foreign objects, specifically metal pieces.
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.
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.
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.
Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, are being recalled after failing dissolution specifications, with olmesartan medoxomil content below specification.
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.
Good Neighbor Pharmacy Extra Strength Antacid, calcium carbonate 750 mg chewable tablets, is being recalled because of the presence of small metallic particles.
PhaseOne Antimicrobial Solution is being recalled because the stainless steel spring inside the sprayer can corrode, releasing trace metallic elements into the solution.
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.
Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Albertsons store-made Muffins Banana Nut Cream Cheese Filled 2 count are being recalled because the contains statement does not declare walnut. Nine units are affected.
Albertsons store-made Shrimp & Surimi Ceviche Fresh is being recalled because the contains statement does not declare sea bream. 315 units are affected.