State
73,596 recalls have nationwide distribution and so reach Pennsylvania. 11,931 additional recalls listed Pennsylvania specifically in their distribution scope.
Of the 11,931 recalls naming Pennsylvania we have scored against our rubric, 1,917 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,385 (28%) are Severe.
Which agencies issued them
These figures cover only the 11,931 recalls whose distribution notice names Pennsylvania specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
BYD is recalling 2023-2024 Ride Type A school buses because an electrical contactor may fail, preventing the wheelchair lift from stopping.
Koenigsegg is recalling 2025-2026 CC850 vehicles because the electronic parking brake may not engage in reverse, increasing crash risk.
Instrumentation Laboratory is recalling 434 units of the HemoslL AcuStar HIT-lgG in vitro diagnostic due to potential for invalid calibration curves or negative mean bias of up to 47% with patient samples.
SI-BONE, Inc. is recalling 100 units of iFuse TORQ Implant System screws because packaging seal integrity testing failed, preventing assurance of sterility.
Jenavalve Technology Inc. is recalling 143 JenaValve Trilogy Delivery Catheters due to a defect that may prevent heart valve deployment.
Beckman Coulter is recalling DxU 840m and 850m Iris analyzers because a check valve defect can cause fluid leaks, creating slip, chemical, and biohazard risks.
PACCAR is recalling specific Kenworth and Peterbilt trucks because remote fuel filter hoses may separate, causing fuel leaks, engine stalls, and increased fire or crash risks.
Medtronic is recalling 18 units of Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.
Ethicon is recalling 1,764 units of PERMA-HAND Silk sutures that were packaged with alcohol-based fluid. The fluid is not part of the product design and could cause surgical delays or treatment failure if used.
Zydus Pharmaceuticals is recalling 70,776 vials of Hydrocortisone Sodium Succinate for Injection due to failed impurities and degradation specifications.
Steris Corporation is recalling 374 units of RAPICIDE PA Part A High-Level Disinfectant because a blocked vented cap may cause the bottle to swell and release vapor or liquid, posing an injury risk.
Houston Rx LLC is recalling 64 vials of Tirzepatide/Niacinamide injection due to a lack of assurance of sterility. The product was distributed nationwide.
Medline is recalling 56 surgical convenience kits because the cannula components may leak or break during use.
Steris is recalling 11,806 units of its RAPICIDE PA high-level disinfectant because a blocked vented cap can cause the bottle to swell and release vapor or liquid, risking user injury.
Medline Industries is recalling 36,199 surgical convenience kits nationwide because cannula components do not meet ISO 80369-7 dimensional requirements, posing a risk of leaking or breaking during use.
Becton Dickinson is recalling 669,200 units of the BD Phoenix Panel NMIC-306 due to potential quality control failures with Klebsiella pneumoniae ATCC BAA-1705.
Cadwell Industries is recalling 23 IOMAX Cortical Modules because a defective circuit board may cause unintended electrical stimulation to patients.
General Motors is recalling 2026 Chevrolet Traverse and GMC Acadia vehicles because insufficient seat welds may fail to restrain occupants in a crash.
Audi is recalling 2024-2025 Q4 E-Tron and Q4 Sportback E-Tron vehicles because the high-voltage battery may fail and cause a fire.
Jenavalve Technology Inc. is recalling 111 units of JenaValve Trilogy Delivery Catheters due to a defect that may prevent heart valve deployment.
Instrumentation Laboratory is recalling 1,414 units of HemoslL AcuStar HIT-lgG(PF-4) in vitro diagnostic reagents due to a potential for invalid calibration curves or negative mean bias of up to 47% with patient samples.
BMW is recalling certain 2018-2020 530e and 740Le vehicles because a loose positive battery cable on the engine starter can spark and cause a fire.
Jenavalve Technology Inc. is recalling 108 units of the JenaValve Trilogy Delivery Catheter due to a defect that may prevent heart valve deployment.
Medtronic is recalling specific Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.
Beckman Coulter is recalling IQ200 SPRINT, SELECT, and ELITE hematology analyzers because a check valve defect may cause fluid leaks, creating slip, chemical, and biohazard risks.