State
73,827 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pier 1 Imports is recalling approximately 140,000 glass knobs sold in the U.S. because they can break during use, posing a risk of laceration.
Wilton Brands is recalling 16,188 bottles of Blue Airbrush Color found to contain mold, yeast, or bacteria. The product was distributed nationwide in the U.S. and Canada.
Boehringer Ingelheim is recalling 2,562 bottles of 75 mg Persantine tablets because 50 mg tablets were found inside the bottles.
Wilton Brands is recalling 13,104 bottles of Yellow Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Wilton Brands is recalling 10,914 bottles of Teal Airbrush Color due to potential contamination with mold, yeast, or bacteria.
Trek Bicycle Corp. is recalling 2014 and 2015 Farley bicycles and framesets because the fork can separate from the steer tube, posing a fall hazard to the rider.
Boehringer Ingelheim is recalling 6,400 bottles of 75 mg Dipyridamole tablets because 50 mg Persantine tablets were found inside the bottles.
TEM Systems Inc is recalling ex-TEM Assay reagents for the ROTEM delta system because customers reported low or empty vials.
Wilton Brands is recalling 13,533 bottles of Pink Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 CMV IgM Assay kits due to reported increased imprecision and high coefficient of variation results.
Pentax of America Inc is recalling video gastroscopes to provide customers with the most recent Operation and Reprocessing Instructions (IFUs).
Wilton Brands is recalling 14,943 bottles of Green Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Wilton Brands is recalling 17,670 bottles of Silver Airbrush Color found to contain mold, yeast, or bacteria. The product was distributed nationwide in the U.S. and Canada.
Zimmer Biomet is recalling 703 Patellofemoral Joint Prosthesis Milling Handpieces because they may be inoperable due to lack of preventative maintenance, potentially delaying surgery.
Wilton Brands is recalling 14,595 bottles of Purple Airbrush Color due to potential contamination with mold, yeast, or bacteria.
Keystone Dental Inc. is recalling 55 units of PrimaConnex Straight Implants because small diameter cover screws were packaged with regular diameter implants.
TZ Medical is recalling Neptune Plus hemostatic pads because the labels incorrectly state they include an antimicrobial barrier.
Wilton Brands is recalling 11,103 bottles of Brown Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Wilton Brands is recalling Red Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Siemens Healthcare Diagnostics is recalling IMMULITE CMV IgM Assay kits due to reported increases in imprecision and high coefficient of variation (CV) values.
Bob's Red Mill is voluntarily recalling one lot of Guar Gum due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.
Wilton Brands is recalling 16,446 bottles of Black Airbrush Color found to contain mold, yeast, or bacteria. The product was distributed nationwide in the U.S. and Canada.
Janssen Ortho L.L.C. is recalling Invokamet tablets because Xarelto prescribing information outserts may be affixed to the bottles instead of the correct Invokamet inserts.
Ortho-Clinical Diagnostics is recalling VITROS HBsAg Controls because signal/cutoff results may increase during the 5-day reconstituted timeframe, potentially affecting performance monitoring.
Winnebago is recalling 2017 View and Navion motorhomes because loose seat mounting bolts may allow seats to detach, increasing injury risk.