State
20,371 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.
Busse Convenience kits containing swab and swabstick products manufactured by Professional Disposables International are recalled by the FDA due to uncertainty regarding the validation of manufacturing test methods.
Busse Hospital Disposables is recalling Universal Nerve Block Tray units (catalog 9779) due to uncertainty regarding test method validation in manufacturing the included swab/swabstick drug products. No illnesses or injuries have been reported.
Busse Convenience kits containing swab/swabstick drug products are recalled due to uncertainty about whether test methods used to validate manufacturing were adequately validated. Distributed nationwide.
Family Dollar Stores is recalling AMBI Skincare Even & Clear Exfoliating Wash because the product was stored outside labeled temperature requirements during manufacturing. No illnesses have been reported.
Family Dollar Stores is recalling Luxury Hygiene Hand Sanitizer due to storage outside of labeled temperature requirements, which may affect product efficacy.
Busse Hospital Disposables is recalling convenience kits containing swab and swabstick drug products due to uncertainty about the adequacy of manufacturing test method validation. Products were distributed nationwide.
Busse Hospital Disposables is recalling convenience kits containing swab products due to uncertainty about adequate validation of manufacturing test methods.
Busse Convenience kits with swab and swabstick drug products are being recalled because the validation of the test methods used during manufacturing is uncertain.
Baxter Healthcare recalled 78 Effluent Sample Bags that were distributed without FDA regulatory clearance. The product was distributed in error across eight states.
Busse Hospital Disposables is recalling Pump Refill Kits nationwide due to uncertainty about whether manufacturing test methods were properly validated. The recall affects 40 units.
Busse Hospital Disposables is recalling Procedure Tray Catalog 1065 nationwide due to uncertain validation of manufacturing test methods for the swab/swabstick drug products inside.
Medtronic is recalling the NIM Vital Patient Interface 4.0 due to a software anomaly identified in the device. The recall affects 29 units distributed worldwide, including in the US and France.
Forest River Aurora travel trailers (2021-2022) have a brake system defect where the breakaway switch may be incorrectly wired, preventing trailer brakes from activating. Dealers will provide free inspection and repairs.
Forest River is recalling certain 2021–2022 Cargo Mate and Continental Cargo Trailers because safety chains don't meet weight rating specifications. A chain failure could cause the trailer to detach from the tow vehicle, increasing crash risk.
Southeast Toyota Distributors is recalling 2020-2022 Toyota 4Runners with 20-inch Black Gunner Wheels due to incorrect load capacity labels that could lead to vehicle overloading and increased crash risk.
Hyundai is recalling 2021-2022 Accent vehicles because a steering column bolt may not be properly secured. This can cause the steering column to detach, resulting in loss of steering control and increased crash risk.
Certain 2022 Toyota vehicles' load capacity labels may fade and become illegible. Illegible labels could allow vehicle overloading, increasing crash risk.
Heartland is recalling certain 2022 Sundance trailers because the 12-volt breaker cover for the slide-out was not installed during production, exposing studs that may cause electrical arcing and fire.
Winnebago is recalling 2021-2022 Micro Minnie and Voyage travel trailers due to cracked LP gas fittings that may leak. Gas leaks near ignition sources pose a fire risk.
Grand Design RV is recalling certain 2022 Solitude, Momentum, Reflection, Imagine, and Transcend travel trailer models with cracked LP gas disconnect fittings that may cause gas leaks and fire risk.
Arcimoto is recalling 2019-2022 FUV, Rapid Responder, Deliverator, and Roadster motorcycles. The charging system may disable at freezing temperatures, potentially causing unexpected stalls and increasing crash risk.
2022 Volkswagen Tiguan vehicles are recalled due to insufficient attachment of the rear hatch spoiler. The spoiler may separate from the vehicle, creating a road hazard and increasing crash risk.
General Motors is recalling 2021 full-size SUVs because third-row seat belts may be entrapped or misrouted behind the seat-folding mechanism, potentially becoming damaged. A damaged seat belt could break during a crash, increasing the risk of occupant injury.
General Motors is recalling certain 2021 Chevrolet Camaro vehicles because the left or right axle shaft may be missing a retaining ring, which could separate during driving and cause loss of power, increasing crash risk.
Tiffin is recalling certain 2021 Phaeton recreational vehicles because the valve stem stabilizer can become loose, allowing the valve stem extender to contact the wheel, which can cause tire pressure loss and increase crash risk.