State
20,189 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.
Microbiologics Inc recalls KWIK-STIK quality control kits contaminated with Aspergillus brasiliensis fungus. Users may observe unexpected fungal growth when using affected control material.
Lupin Pharmaceuticals recalls Rifampin Capsules USP 300mg nationwide due to subpotency—the drug contains less active ingredient than labeled. Affected lot: A201064, expiring March 2024. 26,352 bottles involved.
Boston Scientific's EndoVive 20Fr PEG kit may have a blocked connector preventing proper guidewire advancement during placement, potentially requiring emergency intervention.
Boston Scientific is recalling 572 EndoVive PEG feeding tube kits due to a blocked lumen in the barb connector that may prevent guidewire advancement during placement, potentially requiring device exchange and increasing risk of complications.
NATCO Pharma Limited is voluntarily recalling 30 bottles of Lansoprazole 15 mg delayed-release capsules due to Current Good Manufacturing Practice deviations. The product was distributed nationwide in the United States.
Johnson Health Tech North America is expanding its recall of Matrix T1 and T3 Series commercial treadmills due to a fire hazard from loose power cords. About 9,700 additional units are affected.
Jugader Zipline Kits sold on Amazon.com from March 2020 through June 2023 are recalled because the stainless-steel cable can break, causing falls. The manufacturer has received 20 reports of cable breakage resulting in nine injuries.
Kia is recalling 76,918 model year 2023 Sportage vehicles with potentially twisted side curtain airbags that may deploy improperly, increasing the risk of injury.
Certain 2025 BMW X1 vehicles have B-Pillar reinforcement plates with insufficient structural strength. This defect may reduce crash protection and increase injury risk.
BMW is recalling certain 2024 BMW X3 and related models due to steering gear that may not have been properly tightened, which can loosen and cause loss of vehicle control. Dealers will replace the steering gear free of charge.
About 19,264 Intimidator and Mahindra UTVs are recalled because the universal joint can fail and sever the brake line, posing a crash hazard. No injuries have been reported. Owners should immediately stop using the vehicles and contact a dealer for free repair.
Jayco is recalling 2023-2024 motorhomes where corrosion in an electrical connector can disable the instrument panel, preventing display of the speedometer and warning lights.
About 1,600 BRS portable liquid fuel bottles with non-child-resistant closures have been recalled due to risk of burn and poisoning to children. The closure does not meet requirements of the Children's Gasoline Burn Prevention Act.
Yoto Mini portable speakers for children ages 3–12 are being recalled because the lithium-ion battery can overheat and catch fire. Consumers should stop using them immediately and contact Yoto for a free replacement charging cable.
Red Land Cotton is recalling approximately 17,400 quilts and quilted shams sold on Amazon.com because pieces of broken needles inside the products pose a laceration hazard. The company has received three reports of consumers being jabbed by sharp metal needles.
Fischer Sports is recalling RC4 Junior Ski Boots because the cuff can rotate and cause the lock mechanism to fail, creating a fall hazard. Consumers should stop using them immediately and contact Fischer for a refund, replacement, or repair.
Innovative Bedding Solutions and SBL are recalling about 1,250 GhostBed Natural mattresses because they violate federal flammability standards and pose a fire hazard. Consumers should stop using the mattresses and contact GhostBed for a free compliance cover.
Delta Cycle and Dimension Stem Raisers can shift during use, causing handlebars to move unexpectedly and creating a fall hazard. About 500,000 units sold nationwide from January 1998 through January 2024.
About 356 Touchat Large Fuzzy Area Rugs sold on Amazon.com violate federal flammability regulations and pose a fire hazard. Consumers should stop using them immediately and contact Touchat for a refund.
SleepNet is updating safety warnings and contraindications for its Mojo Non Vented Full Face Mask due to magnet content. All 11,874 affected units are subject to this warning update.
SleepNet Corporation is recalling Mojo 2 Full Face CPAP masks (1,268 units worldwide) to update contraindications and warning language due to magnets in the masks. The FDA classified this as a Class I recall.
SleepNet Corporation is recalling Mojo 2 Full Face Non Vented Masks due to magnets in the device and updated contraindications and warnings. The recall affects 2,107 units distributed worldwide.
SleepNet Corporation is recalling 23,042 Mojo Full Face CPAP masks worldwide because the masks contain magnets that require updated contraindications and warning language.
SleepNet Corporation is recalling 2,787 units of the Mojo 2 Full Face Vented Mask due to updates needed for contraindications and warning language regarding magnets in the device. Worldwide distribution.
SleepNet Corporation is recalling the iQ 2 Nasal Vented Mask due to magnets requiring updated contraindication and warning language. Approximately 2,477 units distributed worldwide are affected.