State
73,213 recalls have nationwide distribution and so reach Pennsylvania. 11,928 additional recalls listed Pennsylvania specifically in their distribution scope.
Of the 11,928 recalls naming Pennsylvania we have scored against our rubric, 1,922 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,870 (24%) are Severe.
Which agencies issued them
These figures cover only the 11,928 recalls whose distribution notice names Pennsylvania specifically. The 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling specific MOPAR side curtain air bag inflators sold as replacement parts for 2011-2020 vehicles due to a manufacturing defect that may cause rupture.
Freedman Seating is recalling specific GO-ES Space Save Foldaway Seats because the recliner mechanism may fail to engage, increasing injury risk during a crash.
Jaguar is recalling certain 2021-2024 E-Pace vehicles because the brake pad wear warning light may not appear when brake pads are worn. This could reduce braking ability and increase crash risk.
Stellantis is recalling 2016 right-hand drive Jeep Wranglers because debris may cause the clockspring to fail, preventing the driver's air bag from deploying in a crash.
Kia is recalling 2022-2024 EV6 vehicles because the Integrated Charging Control Unit may fail, stopping the 12-volt battery from charging. This loss of drive power increases crash risk.
Honeywell is recalling about 29,000 System Sensor L-Series low frequency fire alarm sounders and strobes because they can malfunction and fail to alert people to a fire. No injuries have been reported, but two units showed low or no sound output during installation.
Chrysler is recalling 2021-2022 RAM ProMaster vehicles due to wiring harness defects that can disable the left taillight and turn signal, increasing crash risk. Dealers will replace the harness free of charge.
About 2,500 U.S. Boiler, New Yorker Boiler, Advantage, FORCE, and Archer brand gas-fired boilers are recalled because the blocked vent switch can fail at altitudes above 5,400 feet, allowing carbon monoxide to accumulate in homes. No injuries have been reported.
Best Buy is recalling about 187,400 Insignia brand air fryers and air fryer ovens sold from November 2021 through November 2023 because the units can overheat, causing handles to melt, glass doors to shatter, and fires.
About 500 Tracker Off Road OX EV vehicles are being recalled due to water entering the lithium-ion battery pack, which can cause a fire. No injuries have been reported.
Frios Gourmet Pops frozen popsicles are being recalled because they contain undeclared egg, an allergen. Consumers with egg allergies may face allergic reactions if they consume these products.
Wegmans Harissa Hummus (10.5 oz) is recalled because it contains undeclared sesame, an allergen. Consumers with sesame allergies who have purchased affected lots should not consume the product.
Avanos Medical is recalling MIC Gastric-Jejunal Feeding Tube Kits because they contain a sterile pre-filled syringe that was subsequently recalled by Nurse Assist. Approximately 10,808 units have been distributed worldwide.
Taylor Fresh Foods recalls COLD CASE roasted street corn salad due to potential Listeria monocytogenes contamination. Affected: 60 cases across 28 states.
Textron is recalling 2024 Cushman Hauler Pro LSV vehicles because a dump bed latch may crack or puncture the battery case, increasing the risk of a fire.
Golden Owl Dried Mango (7 oz) is recalled due to undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.
Taylor Fresh Foods is recalling Marketside Bacon Ranch Crunch Chopped Salad Kits due to potential Listeria monocytogenes contamination. Affected products with best-by dates on or before Feb 21, 2024 were distributed to 28 states.
T Marzetti Co is recalling Chick-fil-A Polynesian Sauce Cups (28g single serve) due to undeclared wheat and soy allergens. The product was distributed across 11 U.S. states.
Avanos Medical is recalling MIC Gastric-Jejunal Feeding Tube Kits containing a sterile pre-filled syringe that was recalled by Nurse Assist. Approximately 53,126 units were distributed worldwide.
ConvaTec Natura Stomahesive ostomy kits contain a 45mm flange but 57mm pouch, creating an incompatible coupling. The mismatch prevents the components from fitting together properly.
Ortho-Clinical Diagnostics is recalling VITROS immunodiagnostic analyzer systems that may aspirate unintended sample containers during processing, potentially causing erroneous test results.
Howmedica Osteonics Corp. is recalling the NO 3 Triathlon TS Plus Tibial Insert due to potential breaches in the sterile packaging. The breaches could compromise product sterility and safety.
A software defect in VITROS 4600 Chemistry Systems causes quality control baselines to not update when users change them, potentially causing erroneous patient results.
A software defect in VITROS XT 3400 Chemistry Systems prevents quality control rules from properly reporting failures in test controls. This may result in erroneous patient test results being reported.
A software defect in VITROS 4600 Chemistry Systems running software versions 3.8.0 or 3.8.1 prevents quality control rules from being flagged or reported correctly, potentially allowing erroneous patient results to be released.