State
73,596 recalls have nationwide distribution and so reach Arizona. 8,391 additional recalls listed Arizona specifically in their distribution scope.
Of the 8,391 recalls naming Arizona we have scored against our rubric, 1,311 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,049 (24%) are Severe.
Which agencies issued them
These figures cover only the 8,391 recalls whose distribution notice names Arizona specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sauer Brands Inc is recalling Saigon Organic Cinnamon jars due to potential Salmonella contamination. The product was sold nationwide and online.
Sauer Brands Inc is recalling specific jars of The Spice Hunter Green Hatch Chile due to potential Salmonella contamination. Consumers should check their pantries for the affected lot.
Sauer Brands Inc is recalling The Spice Hunter Gourmet Sesame Seeds due to potential Salmonella contamination. The product was distributed nationwide and online.
Sauer Brands Inc is recalling The Spice Hunter Everything Bagel Crunch due to potential Salmonella contamination. The product was distributed nationwide and online.
Vascular Solutions, Inc. is recalling 89,121 Langston Dual Lumen Catheters because the inner lumen may separate from the hub during pressure injection.
Sauer Brands Inc is recalling specific jars of The Spice Hunter Black Pepper and Fine Black Pepper due to potential Salmonella contamination.
ICU Medical is recalling specific lots of 112-inch burette sets because a manufacturing defect may prevent a proper seal with the NanoClave spike.
Bien-Air Surgery is recalling 1,120 foot pedals because an internal magnet may detach, causing the motor to start unattended and become unstoppable.
Acella Pharmaceuticals is recalling NP Thyroid 15 tablets because FDA analysis found the levothyroxine content was less than labeled.
ICU Medical is recalling specific lots of smallbore intravascular administration sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.
Sauer Brands Inc is recalling specific lots of The Spice Hunter Herbs De Provence due to potential Salmonella contamination.
Vascular Solutions, Inc. is recalling 1,745 Langston Dual Lumen Catheters because the inner lumen may separate from the hub during pressure injection.
ICU Medical is recalling specific lots of NanoClave intravascular administration sets because a manufacturing defect may prevent a proper seal with the spike.
ICU Medical is recalling specific lots of 7-inch smallbore extension sets because a manufacturing defect may prevent the NanoClave from sealing properly.
ICU Medical is recalling specific lots of intravascular administration sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.
ICU Medical is recalling specific lots of smallbore pressure infusion extension sets due to a potential manufacturing defect that may inhibit a proper seal.
ICU Medical is recalling specific lots of NanoClave Connectors because a manufacturing defect may prevent a proper seal with the spike.
Smith & Nephew is recalling HEALICOIL absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
ICU Medical is recalling specific lots of Smallbore Trifuse Extension Sets because a manufacturing defect may prevent the NanoClave spike from sealing properly.
Smith & Nephew is recalling OSTEORAPTOR absorbable suture anchors because improper or incomplete packaging seals may breach the sterile barrier.
ICU Medical is recalling specific lots of NanoClave administration sets because a manufacturing defect may prevent the NanoClave from sealing properly.
ICU Medical is recalling specific lots of smallbore extension sets because a manufacturing defect may prevent the NanoClave from sealing properly.
Smith & Nephew is recalling TWINFIX 6.5mm absorbable suture anchors because improper packaging seals may breach the sterile barrier.
Smith & Nephew is recalling TWINFIX ULTRA PLLA/HA 5.5 W/3 UB Absorbable Suture Anchors because improper or incomplete packaging seals may breach the sterile barrier.
ICU Medical is recalling specific lots of 7-inch smallbore extension sets because a manufacturing defect on the NanoClave surface may inhibit a proper seal.