State
72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Merit Medical is recalling the 16F Dual Valved Splittable Sheath Introducer in bulk non-sterile form because a design defect may prevent it splitting as intended.
Philips Respironics is recalling the Trilogy Evo Universal ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Philips Respironics is recalling the Trilogy Evo ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Ajinomoto Foods North America Inc. is recalling Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed (1 lb. bags) due to glass fragments 1–3 cm long and 2–4 mm wide found in the product.
Bakkavor is recalling Basil Pesto & Mozzarella Pizza due to metal fragments discovered in the product. The contamination originated from roasted tomatoes supplied by an ingredient supplier.
Philips Respironics is recalling the Trilogy EV300 ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Merit Medical is recalling DuraMax Chronic Hemodialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
Isuzu is recalling 2025-2027 commercial trucks because wire harnesses may chafe, causing engine stalls, brake failures, or fires.
Erbe USA is recalling the Flexible Cryoprobe REF 20402-410 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Navajo Manufacturing is recalling the Handy Solutions Neck & Shoulders Heating Pad because folding it during use raises power density in the folded area, causing excessive temperatures the limit device cannot sense.
Philips Respironics is recalling the Trilogy Evo O2 ventilator because using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the volume the patient receives.
Bakkavor is recalling roasted tomato and parmesan focaccia bread sold under multiple retail brands due to metal fragments discovered in the products. The metal originated from roasted tomatoes supplied by an ingredient supplier.
Merit Medical is recalling CentrosFLO Hemodialysis Catheters because a design defect in the 16F dual-valved splittable sheath introducer may prevent it splitting as intended.
SiluetaYa Mexican Tejocote Roots Supplement Pieces (7g bottles, Lot US1220) are recalled because the product contains yellow oleander, a toxic substance. The product was distributed online to consumers in AZ, CA, NM, NY, TX, and UT.
Erbe USA is recalling the Flexible Cryoprobe REF 20402-411 because the probes may rupture or burst during activation. The FDA has classified this recall as Class I.
Olympus is recalling PK Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.
Ajinomoto Foods North America Inc. is recalling Tai Pei Shrimp Fried Rice due to glass fragments found in the product. Glass pieces measuring 1–3 cm long and 2–4 mm wide pose a choking and injury risk.
American Laboratories is recalling Pepsin 1:10,000 Powder (10 kg, Item #FTI-G0193-00, Lot Code 00560021) distributed to wholesale accounts due to potential Salmonella contamination.
Olympus is recalling Everest Bipolar Cutting Forceps model 3005 because a supplier did not adequately validate the welding process, and defective welds can cause the jaw to break during clinical use.
Macleods Pharma USA is recalling one lot of Levothyroxine Sodium Tablets USP 150 mcg because the product is subpotent.
Straumann is recalling Custom Abutment AS Ti for Straumann RC because a material mix-up meant titanium abutments were manufactured from TAN bar material instead of Titanium Grade 4.
Ajinomoto Foods North America Inc. is recalling Ajinomoto Green Gyoza Vegetable & Edamame Dumplings due to the presence of glass fragments (1–3 cm long and 2–4 mm wide) in the product.
Savannah Bee Company is recalling Honey BBQ Sauce Mustard bottles containing an undeclared different flavor product with soy and wheat allergens not listed on the label.
Chiesi USA is recalling three lots of Curosurf (poractant alfa) Intratracheal Suspension for lack of assurance of sterility.
I.T.S. GmbH is recalling the Fibula Plate PROlock with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.