State
73,509 recalls have nationwide distribution and so reach Hawaii. 2,772 additional recalls listed Hawaii specifically in their distribution scope.
Of the 2,772 recalls naming Hawaii we have scored against our rubric, 333 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 715 (26%) are Severe.
Which agencies issued them
These figures cover only the 2,772 recalls whose distribution notice names Hawaii specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sutphen is recalling 2020 Fire trucks because pressure in the power steering pump may break the shaft seal, causing a loss of steering assist and increasing crash risk.
Volkswagen is recalling certain 2021 Atlas and 2020-2021 Cross Sport vehicles whose air conditioning drain tube can become blocked, allowing water to damage the air bag control module and potentially trigger inadvertent air bag deployment.
Simply Delicious, Inc. is recalling Bobo's Almond Butter Protein Bars (2.2 oz.) because they contain undeclared peanuts, posing a risk to consumers with peanut allergies.
Jayco recalls certain 2021-2022 motorhomes with defective seat belt retractors that may fail to secure child restraint systems during crashes. Dealers will replace the retractors free of charge.
Zhejiang Kindly Medical Devices is recalling Henry Schein Safety Blood Collection Needles due to potential difficulty activating the safety mechanism. Affected lot numbers distributed nationwide.
Daimler Trucks North America is recalling Freightliner 108SD, 114SD, Coronado, and Western Star trucks from model years 2012-2022 due to unapproved tires and rims that do not meet federal safety standards.
McKesson PREVENT HT Safety Winged Blood Collection Needles may have difficulty activating their safety mechanism. The recall affects units distributed nationwide.
Z-Medica is recalling 2400 units of QuikClot Combat Gauze due to potential packaging seal failures that could compromise sterile barrier integrity. Affected lot 12645 was distributed nationwide.
Philips Azurion Interventional X-Ray Systems (software 2.1.x) may experience imaging lock-up when operators simultaneously press both the APC and Float Tabletop buttons.
Nationwide recall of McKesson PREVENT HT Safety Blood Collection Needles (22G 1 1/4 inch) due to potential difficulty activating the safety mechanism. The protective feature may fail to engage properly during use.
McKesson PREVENT HT Safety Blood Collection Needles are being recalled due to potential difficulty in activating the safety mechanism. The recall affects needles distributed nationwide, including specific lot numbers with expiration dates through May 2025.
Toyota is recalling 2022 Sienna and Sienna Hybrid vehicles with eight-passenger seating because an incorrect seat belt webbing guide may cause the belt to tear during a crash.
McKesson PREVENT HT blood collection needles with specific lot numbers may have difficulty activating their safety mechanism. Healthcare facilities should contact the manufacturer for replacement guidance.
Baxter's Hemodialysis Delivery System may incorrectly revert to old prescription values when operators change prescriptions after filter changes, potentially resulting in incorrect treatment parameters.
Henry Schein safety blood collection needles may have difficulty activating their safety mechanism, potentially increasing needlestick injury risk. Affected lots were distributed nationwide with expiration dates through late 2025.
Ascend Laboratories LLC is recalling Cefixime Capsules 400 mg nationwide due to failed impurities and degradation specifications. The affected lot is Lot 20140282 with an expiration date of December 2021.
Sun Pharmaceutical is recalling Tadalafil Tablets USP 20 mg due to use of an incorrect grade of Crospovidone during manufacturing. The recall affects 36,786 bottles distributed to one distributor.
Sun Pharmaceutical Industries is recalling Tadalafil 5 mg tablets (Lot # DNC1127A) because an incorrect grade of Crospovidone was used during manufacturing. The product was distributed to one distributor who may have further distributed it nationwide.
Precision Dose Inc. is recalling Acetaminophen Oral Suspension (325 mg/10.15 mL) due to contaminated raw ingredient used in manufacturing. The recall affects 151,100 unit dose cups distributed nationwide for hospital use.
Precision Dose Inc. is recalling 166,920 unit dose cups of Acetaminophen Oral Suspension 160 mg/5 mL (Lot 503670) distributed nationwide due to cGMP deviations involving contaminated raw ingredient used in manufacturing.
Cummins is recalling 2019-2021 C70D2RE and C100D2RE generator sets because improperly manufactured circuit breakers may fail to protect circuits, increasing fire and injury risks.
Jayco is recalling 2020-2022 Anthem, Embark, Reatta, and Reatta XL motorhomes because rear suspension fasteners may loosen or break, increasing crash risk.
Jayco recalls certain 2021 Entegra Cornerstone motorhomes with a power steering pump defect that may result in loss of steering assist. Owners should contact Jayco for free pump replacement to prevent increased crash risk.
M H Eby is recalling 2020-2022 EBY Generation trailers because missing white conspicuity tape on the top rear corners reduces visibility to other drivers.
Altec is recalling 2012-2016 AT200A aerial devices because cracks in the mounting frame legs may cause the side plate to break, increasing injury risk.