State
73,738 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,596 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 2,534 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,596 recalls whose distribution notice names Indiana specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Flowonix Medical Inc is recalling US Clinical 20mL Programmable Pumps because a firmware anomaly may prevent the device from sending error codes or audible alarms during valve system issues.
Flowonix Medical Inc is recalling Prometra II implantable infusion pumps because a firmware anomaly may prevent the device from sending error codes or audible alarms.
Pfizer is recalling 141 bottles of Caduet tablets because defective bottle rims may have allowed moisture to enter, potentially compromising the medication.
Teva Pharmaceuticals USA is recalling 17,436 bottles of Methylphenidate Hydrochloride Extended-Release tablets because the product bottles may be missing desiccant.
Prollenium Medical Technologies is recalling 48,457 kits of Revanesse Versa because the product is labeled with an 18-month expiration date, but it is only approved for 12 months.
Contract Pharmacal is recalling Major Extra Strength Acetaminophen tablets because a foreign prenatal tablet was found in a bottle.
Implant Direct is recalling 78 Legacy 3 dental implants because some packages contain incorrect cover screws and extenders, which may delay surgery or require new procedures.
Pfizer is recalling 128 bottles of Caduet (amlodipine and atorvastatin) because defective bottle rims may have caused inadequate foil sealing, potentially compromising moisture protection.
Lupin Pharmaceuticals is recalling 6,294 bottles of Memantine Hydrochloride Extended Release Capsules because they failed to meet dissolution specifications during stability testing.
C.R. Bard Inc. is recalling 1,300 units of the Bard Intra-abdominal Pressure Monitoring Device due to leaks or disconnects that may cause inaccurate readings.
Sugar Foods Corporation is recalling specific lots of granulated pure cane sugar sold under Ahold, N'Joy, and Speedway brands because the product may be contaminated with foreign material.
CooperVision is recalling specific lots of Vertex Toric contact lenses because they were manufactured with an incorrect power.
Teva Pharmaceuticals is recalling specific bottles of Methylphenidate Hydrochloride Extended-Release tablets because they may be missing the desiccant packet.
GSK is recalling Theraflu Cough Relief packets because the label lacks a warning for people on sodium-restricted diets.
CooperVision is recalling 216 units of Vertex Toric contact lenses because they have an incorrect power than expected.
American Health Packaging is recalling 973 cartons of Raloxifene Hydrochloride 60 mg tablets due to low dissolution results found during stability testing.
Taewoong Medical Co., Ltd. is recalling 178 esophageal stents because the Instructions for Use (IFUs) shipped with the devices were misprinted.
Par Pharmaceutical is recalling 9,936 cartons of Frovatriptan Succinate Tablets, 2.5mg, because they are labeled with an incorrect expiration date.
Jayco is recalling 2013-2015 Fifth Wheel Seismic and 2015 Pinnacle trailers because they were built with 6,000lb axles instead of the intended 7,000lb axles.
Bentley is recalling 2018-2020 Bentayga vehicles because side curtain air bags may not inflate properly in a crash, increasing injury risk.
PACCAR is recalling 2020 Kenworth T370 trucks because a missing relay valve may increase brake activation time, lengthening stopping distance and increasing crash risk.
Mercedes-Benz is recalling 2019-2020 G 550 and AMG G63 vehicles because a faulty electrical resistor may deactivate Electronic Stability Program and Anti-lock Brake System.
Kia is recalling 2006-2010 Sedona and 2007-2009 Sorento vehicles because moisture in the ABS module can cause an electrical short and engine compartment fire.
Mercedes-Benz is recalling specific 2020-2021 models because instrument cluster software may deactivate interior switch illumination, increasing crash risk.
Chrysler is recalling 2019 Ram 1500 4WD trucks because a transfer case gear may be installed incorrectly, potentially causing a sudden loss of power or loss of the Park function.