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.
Ford is recalling certain 2020-2021 F-150 and Super Duty trucks because the windshield may not be properly bonded, risking detachment in a crash. Dealers will remove and reinstall the windshield at no cost.
Backcountry Access Tracker4 Avalanche Transceivers are being recalled because the toggle switch can separate from the unit and prevent it from switching to search mode, which could prevent rescuers from locating a buried skier.
Joey Clothing is recalling about 15,930 children's robes sold online because they fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries.
Newmar is recalling 2020-2022 motorhomes due to steering gear mounting bolts that may back out, potentially causing loss of steering control. Owners should contact Newmar for a free replacement of affected bolts.
Electrolux is recalling about 367,500 Frigidaire and Electrolux refrigerators because the ice level detector arm in the ice maker can break apart and fall into the ice bucket, creating a choking hazard.
Autocar is recalling certain 2018-2021 Xpeditor vehicles because the turbocharger heat shield may fail and detach, creating a road hazard. Dealers will replace the component free of charge.
Demdaco microwavable bowl holders can char and catch fire when microwaved for the recommended time. The company received three reports of charring incidents and is offering refunds.
Mazda is recalling certain 2020-2021 CX-30 vehicles because the power liftgate may partially lower unexpectedly when parked on uphill slopes, risking injury to those accessing the rear storage area.
Target is recalling about 120,000 children's pajama sets because they fail to meet federal flammability standards for sleepwear, posing a burn injury risk to children. Consumers should return the pajamas to Target for a full refund.
BMW is recalling certain 2021 X5 sDrive40i and X5 xDrive40i vehicles because the right front brake disc may have incorrect fasteners that could loosen over time, affecting vehicle control and increasing crash risk.
Communicorp is recalling about 600,000 six-inch Aflac plush promotional ducks distributed to Aflac employees and customers from February 2009 through March 2021. The ducks contain phthalates and lead levels that exceed federal standards and pose a risk if ingested by young children.
Certain 2019-2021 Autocar Xpeditor and 2021-2022 Legend vehicles with a 7-inch display may experience restarts that hide critical warning lights. Dealers will replace the display free of charge.
Asweets is recalling about 13,300 Wonder & Wise baby activity walkers because rubber rings on the rear wheels can detach, posing a strangulation hazard to young children. No injuries have been reported.
The FDA is recalling approximately 4,449 Sara Plus Active Floor Lift devices due to a fire hazard. The devices may emit smoke or ignite, posing a risk to users and staff.
Teleflex Medical is recalling Gibeck brand respiratory filters due to reports of torn corrugated breathing tubes. No injuries have been reported.
Olympia Compounding Pharmacy is recalling 9,102 vials of Phenylephrine 1 mg/mL due to lack of assurance of sterility. The affected vials were distributed nationwide in the United States, Puerto Rico, and US Virgin Islands.
Olympia Compounding Pharmacy recalls a multi-drug injectable compound (lot B41C22-22) due to inability to assure sterility. The recall affects 1,159 vials distributed nationwide.
Olympia Compounding Pharmacy is recalling pharmaceutical diluent vials due to lack of sterility assurance. The product was distributed nationwide in the USA, Puerto Rico, and US Virgin Islands.
Accriva Diagnostics distributed an unclearred variant of the VerifyNow P2Y12 platelet test that displays different results than the FDA-cleared device. A correction formula has been provided to healthcare providers.
Olympia Compounding Pharmacy recalls Methylcobalamin 5 mg/mL injectable due to lack of assurance of sterility. Approximately 12,800 vials were distributed nationwide.
Devicor Medical Products is recalling 90 HydroMARK Breast Biopsy Markers due to mismatched patient labels that incorrectly identify the product model. The small patient label identifies the device as model 4010-05-08-T3, while the correct model is 4010-05-08-T4.
Medtronic has recalled the Percept PC BrainSense Implantable Neurostimulator Model B35200 due to communication failures with programmer systems. The device cannot reliably communicate with clinical or patient programmer systems.
Olympia Compounding Pharmacy is recalling Formula F2, a multi-ingredient injectable medication, because the manufacturer cannot assure sterility. The recall affects 72 vials distributed nationwide.
Olympia Compounding Pharmacy is recalling 1,306 vials of Pyridoxine 100 mg/mL injectable due to lack of assurance of sterility. The multi-dose vials were distributed nationwide and may pose infection risk if administered.
ConvaTec is recalling 600 market units of SUR-FIT Natura S4S Durahesive Wafer due to skin barrier delamination. The wafer's layers or tape borders may fail to maintain proper seal, potentially affecting skin protection.