State
73,366 recalls have nationwide distribution and so reach Hawaii. 2,771 additional recalls listed Hawaii specifically in their distribution scope.
Of the 2,771 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 2,771 recalls whose distribution notice names Hawaii specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
E S Foods is recalling 65550 5 Days Meal Kits nationwide because animal crackers may contain bronze metal shavings. Consumers should not consume the affected products.
Heartland Recreational Vehicles is recalling 2023 BIGHORN and BIG COUNTRY fifth wheels with incorrect tire information on federal certification labels, which could allow improper tire installation and increase crash risk.
Bio-Rad is recalling BioPlex 2200 Anti-CCP Reagent Pack, Lot 301481, because the test's specificity is lower than claimed, which may increase false positive results. The diagnostic kit was distributed worldwide including the US, Canada, and several European countries.
Coloplast is recalling Titan Touch Scro Zero Ang 20cm penile prostheses due to decreased wall thickness that could cause premature pump failure. Patients should contact their healthcare provider for guidance.
Coloplast is recalling Titan Touch Scro Zero Ang 16cm prostheses (Lot 8840677) due to decreased wall thickness that may cause premature pump failure. Affected devices were distributed worldwide, including throughout the US.
Philips CombiDiagnost R90 X-ray systems (Model Numbers 709030 and 709031) may experience electrical fire in the main cabinet if exposed to overvoltage or power surge.
Coloplast is recalling the Titan 0-Deg Infrapubic 20 Cm inflatable penile prosthesis due to reduced wall thickness in the pump that could cause premature failure. No injuries have been reported.
Covidien's Step Bladeless Trocars (Model S101010, Lot P2G0069) are being recalled due to a sterilization process failure that may have resulted in unsterile instruments. Use of affected units may lead to infection or vision loss in eye procedures.
E S Foods is recalling 1,044,918 meal kits containing animal crackers distributed nationwide due to potential bronze metal shaving contamination. No illnesses have been reported.
Coloplast is recalling Titan Touch inflatable penile prostheses with reduced pump wall thickness, which could cause premature failure during use. The defect affects 8 units distributed across the US and multiple European countries.
Merit Medical Systems inadvertently distributed 17 Flex-Neck Catheter External Repair Kits intended for design verification testing to customers in Maryland, Michigan, Ohio, and Texas.
Coloplast is recalling certain Titan NB Infra Zero Ang 16cm inflatable penile prostheses due to thinner-than-standard pump wall thickness that could lead to premature pump failure.
E S Foods is recalling 1,044,918 meal kits sold nationwide. The animal crackers in these kits may contain bronze metal shavings, which could cause injury if consumed.
Philips ProxiDiagnost R90 X-ray systems may experience electrical fires if exposed to overvoltage or power surges. The recalled systems affect 243 units distributed nationwide and globally.
Covidien, LP is recalling chromic gut absorbable sutures due to sterilization failure that may leave product unsterile, creating risk of infection or vision loss in eye surgery.
E S Foods is recalling 61490 Cheese Cup with 2 Grains meal kits because the animal crackers may contain metal shavings. These products were distributed nationwide.
Impossible Foods is recalling 128,029 cases of Impossible Chicken Nuggets nationwide due to potential wood contamination. The products should not be consumed.
Philips DigitalDiagnost C50 ceiling suspensions may descend unexpectedly if annual preventive maintenance is not performed, potentially injuring patients and healthcare workers.
Coloplast is recalling 15 units of the Titan Touch Infr Zero Ang inflatable penile prosthesis (Lot Numbers 8849582, 8849603, 8904185) worldwide due to decreased wall thickness that may cause premature pump failure.
Coloplast Manufacturing is recalling the Titan 0-Deg Scrotal 18 Cm inflatable penile prosthesis (25 units) due to decreased wall thickness that may cause premature pump failure. Patients with affected lot numbers should contact their healthcare provider.
Sun Pharmaceutical is recalling Norepinephrine Bitartrate Injection due to a chemical impurity exceeding specification limits detected during routine monitoring. The recall affects 16,450 vials distributed nationwide.
Agilent Technologies is recalling 560 sample collection kits that were distributed with instructions for use the FDA had not approved.
TIPPCON LLC is recalling Perrona Hot Sauce Original with Chiltepin Peppers due to mold growth on the outside of the bottle. The affected product was distributed nationwide.
Pine Pharmaceuticals is recalling 932 syringes of Bevacizumab 2.5 mg/0.1 mL due to incorrect lot number labeling on the primary packaging. The affected lot (#66377, expiration 06/28/2023) was distributed nationwide.
Angiodynamics recalls NanoKnife 5-Probe Procedure Packs due to a programming error affecting RFID function. The probes may not be recognized by the NanoKnife generator, potentially delaying surgical procedures.