State
20,188 recalls have nationwide distribution and so reach Pennsylvania. 0 additional recalls listed Pennsylvania specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Pennsylvania consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
General Motors is recalling certain 2022 Chevrolet Silverado and GMC Sierra trucks with an accessory sport bar. The high-mounted brake light may not function or may be blocked, reducing visibility to other drivers and increasing crash risk.
SA Consumer Products is recalling Sanctuary Quick Access and Sports Afield Biometric Firearm Safes because the biometric lock can be opened by unauthorized users, posing a serious injury hazard and risk of death. No injuries have been reported.
Daimler Trucks is recalling certain 2022 Freightliner Cascadia trucks because the electronic parking brake may fail to engage when turned off, risking vehicle rollaway. Owners should contact dealers for free repair.
Chrysler recalls 2023 RAM 1500, 2500, and 3500 vehicles with a transmission control unit weld defect that may cause transmission fluid to leak onto electrical components, resulting in loss of drive power or park function.
Gulf States Toyota is recalling 2022-2024 Toyota Highlander L and Highlander LE vehicles with the Blackout Package because their installed tires have insufficient load rating and may fail, increasing crash risk.
About 1,160 sling carriers sold on Walmart.com through Joybuy Marketplace Express are recalled due to violations of federal safety standards. The carriers pose suffocation and fall hazards to infants because they lack required structural integrity, occupant retention, and proper restraint systems.
Spectrum Brands is recalling about 102,000 units of FURminator deShedding Ultra Premium Dog Conditioner (1 Gallon) because the product can contain Pseudomonas aeruginosa bacteria, which poses a serious infection risk to people with weakened immune systems or external medical devices.
GM is recalling 2024-2025 Chevrolet Corvettes because front seat belt retractors may lock and become inaccessible. This prevents seat belts from restraining occupants in a crash, increasing injury risk.
Salewa USA recalls Wild Country Ropeman 1 ascenders because the teeth can fail to engage, making it difficult or impossible to ascend. About 7,700 units sold in the United States since December 2022.
Medline endotracheal tubes with subglottic suctioning may have inflation tubes that detach or tear and suction pumps that disconnect, risking loss of ventilation control.
Revive Rx Pharmacy recalls 751 vials of compounded tirzepatide (Lot #748127) labeled to contain tirzepatide but actually filled with testosterone cypionate. Patients receiving this medication may take the wrong drug with serious health consequences.
Alcon is recalling about 19,867 ClearCut S and A-OK ophthalmic surgical knives worldwide due to an increase in complaints about blade sharpness.
Stryker Neurovascular is recalling 81 neurovascular devices due to inadequate endotoxin testing. The devices may contain excessive endotoxin levels, which can cause fever, shock, and aseptic meningitis.
Escape Trailer is recalling 2021-2022 Escape travel trailers (models 17, 19, 21, and 5.0TA) due to cracked quick disconnect fittings in the LP gas system that may cause a gas leak and fire hazard.
Dr. Reddy's Laboratories recalls Zoledronic Acid Injection 5mg/100mL due to lack of sterility assurance and leaking vials. Lot #G3000010 with 13,880 vials was distributed nationwide.
Mirion Technologies is recalling the Captus 4000e Thyroid Uptake System due to complaints of unexpected collimator detachment. Affected users should contact the manufacturer for guidance.
Alcon is recalling ClearCut Dual Bevel Sideport and A-OK Corneal/Scleral V-Lance ophthalmic surgical knives due to increased complaint reports about sharpness. Approximately 427,764 units are affected worldwide.
Altec is recalling 2021-2023 aerial devices, digger derricks, and related equipment because water can leak into strobe lights, causing electrical short-circuits that increase fire risk. No injuries have been reported.
Maribel's Sweets is recalling Mother's Day ganache boxes due to undeclared coconut. Consumers with coconut allergies face risk of allergic reaction.
Imprimis NJOF, LLC is recalling Dexamethasone-Moxifloxacin-Ketorolac intraocular injections (38,060 vials) due to lack of assurance of sterility. The affected lots were distributed nationwide.
Mirion Technologies is recalling 1,275 units of the Captus 4000e Thyroid Uptake System worldwide due to complaints of unexpected collimator detachment.
Stryker Neurovascular is recalling Trevo NXT neurovascular intervention devices because they did not receive adequate endotoxin testing during manufacturing. High endotoxin levels may cause fever, shock, or aseptic meningitis.
Certain 2021–2023 Jeep Grand Cherokee models have an incorrectly assembled steering column intermediate shaft that may disconnect and cause loss of steering control, increasing crash risk. Chrysler is offering free inspection and replacement.
Alcon is recalling approximately 29,190 V-Lance ophthalmic surgical knives due to reports of blade sharpness defects. Affected instruments are distributed worldwide, including as components in Alcon Custom Pak surgical procedure packs.
Imprimis NJOF, LLC recalls Moxifloxacin intraocular injection vials nationwide due to lack of sterility assurance. The 18,980 affected vials (lot 23OCT013) should not be used.