The Recall Desk

State

Pennsylvania product recalls

72,820 recalls have nationwide distribution and so reach Pennsylvania. 11,910 additional recalls listed Pennsylvania specifically in their distribution scope.

What the numbers show

Total
11,910
Critical
1,922
Severe
2,864
Most recent
2026-09-02

Of the 11,910 recalls naming Pennsylvania we have scored against our rubric, 1,922 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,864 (24%) are Severe.

These figures cover only the 11,910 recalls whose distribution notice names Pennsylvania specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

701–725 of 84730

  • ModerateFDA (Drugs)·D-0688-2026·2026-07-22

    CAREone Earwax Removal Drops Recalled for Subpotent Active Ingredient

    CAREone Earwax Removal Drops (Carbamide Peroxide 6.5%) are recalled because the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, making it ineffective.

    Product
    CAREONE EARWAX REMOVAL DROPS — CAREONE EARWAX REMOVAL DROPS (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0677-2026·2026-07-22

    Nystatin Cream Recall Due to Low Potency Test Results

    Padagis US LLC is recalling Nystatin Cream USP (100,000 USP units) because long-term stability testing found assay results below specification, meaning the product may contain less active ingredient than labeled.

    Product
    NYSTATIN — NYSTATIN (NYSTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0680-2026·2026-07-22

    Quality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall

    Bell Pharmaceuticals is recalling Quality Choice Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotent drug content, with assay levels significantly reduced (approximately 0.6% versus expected 6–7%) and low pH levels.

    Product
    QUALITY CHOICE EARWAX REMOVAL KIT — QUALITY CHOICE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0681-2026·2026-07-22

    TopCare Earwax Removal Kit Recalled for Subpotent Drug Content

    Bell Pharmaceuticals is recalling TopCare Earwax Removal Kit (Carbamide Peroxide 6.5%) because the drug is subpotent with significantly reduced active ingredient (~0.6% vs. expected 6–7%) and low pH. The affected product was distributed nationwide.

    Product
    TOPCARE EARWAX REMOVAL KIT — TOPCARE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0684-2026·2026-07-22

    Good Neighbor Pharmacy Earwax Removal Drug Recalled for Low Potency

    Bell Pharmaceuticals is recalling Good Neighbor Pharmacy Earwax Removal (Carbamide Peroxide 6.5%) due to subpotency—the active ingredient concentration is significantly reduced from expected levels, and the product has a low pH.

    Product
    GOOD NEIGHBOR PHARMACY EARWAX REMOVAL — GOOD NEIGHBOR PHARMACY EARWAX REMOVAL (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1152-2026·2026-07-22

    Liquid Hope Organic Meal Replacement Formula Subpotent Vitamin A Recall

    Nutricia North America is recalling Liquid Hope Organic Whole Foods Meal Replacement Peptide Formula Berry Medley because the product contains less vitamin A than labeled. A testing laboratory used an incorrect method that overstated the vitamin A concentration.

    Product
    functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ (341g) case UPC 8 57858 00453 3, package UPC 8 57858 00450 2
    Category
    Food
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-2737-2026·2026-07-22

    Medline Kits with Zimmer Biomet Mixing Bowls and Spatulas Recalled

    Medline Industries is recalling 163 kits containing Zimmer Biomet mixing bowls and spatulas due to seal defects that risk sterility breach during surgical procedures.

    Product
    Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2746-2026·2026-07-22

    Tosoh ST AIA-Pack Testosterone Diagnostic Test Kit Recall

    Tosoh Bioscience is recalling ST AIA-Pack Testosterone test kits due to low-quality control results that could produce falsely elevated or falsely low testosterone measurements, potentially leading to unnecessary testing or delayed diagnosis.

    Product
    ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers, Model Number 0025204
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2742-2026·2026-07-22

    Photera 400 Phototherapy Device Recalled for Incorrect UV Sensor Calibration

    Daavlin Distributing Company is recalling the Photera 400 phototherapy device because the UV sensor calibration is calculating incorrectly, resulting in lower output levels than intended.

    Product
    Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2733-2026·2026-07-22

    Papablic Replacement Brush Heads Recalled for Potential Breakage

    Papablic Inc is recalling certain Papablic18B replacement brush head packs because the brush heads may break during use.

    Product
    Papablic Replacement Brush Heads. Model Number: Papablic18B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2740-2026·2026-07-22

    Rio II Nasal Pillows Interface Packaging and Labeling Discrepancy Recall

    3B Medical, Inc. is recalling Rio II Nasal Pillows Interface devices due to packaging and labeling discrepancies involving product size identification and device identifiers. The affected models are RII1001 (Small), RII1002 (Medium), and RII1003 (Large).

    Product
    Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number: RII1001 (Small), RII1002 (Medium), RII1003 (Large) Software Version: N/A Product Description: Nasal pillows interface intended for use with positive airway pressure therapy devices. The de
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V470000·2026-07-21

    Ford Recalls 2025-2027 Explorer and Lincoln Aviator for Seat Recline Issue

    Ford is recalling 76,748 2025-2027 Explorer and Lincoln Aviator vehicles because an unoccupied driver's seat may recline unintentionally, potentially trapping a second-row occupant.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·26V469000·2026-07-21

    Ember Recalls 2027 Travel Trailers Due to Incorrect VIN Labels

    Ember is recalling 2027 E-Series, Touring, and Overland travel trailers because the Federal Certification Label may list the wrong VIN, which could prevent owners from recognizing safety recalls.

    Product
    EMBER — EMBER E-SERIES, TOURING EDITION, OVERLAND SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V467000·2026-07-20

    Blue Bird Recalls 2022-2027 Vision Transit Buses for Brake Line Damage

    Blue Bird is recalling 2022-2027 Vision transit buses because an exhaust hanger pin may damage the hydraulic brake line, causing leaks and increasing fire or crash risks.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V466000·2026-07-20

    Blue Bird Vision School Buses Recalled Due to Brake Line Fire and Crash Risk

    Blue Bird is recalling certain 2022-2027 Vision school buses because an exhaust hanger cotter pin may damage hydraulic brake lines, causing leaks that increase the risk of fire or crashes.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V463000·2026-07-17

    Altec Recalls 2024-2026 AT Series Vehicles Due to Bearing Fastener Defect

    Altec is recalling 2024-2026 AT Series vehicles because turntable rotation bearing fasteners may not have been heat treated properly, posing a risk of component separation and injury.

    Product
    ALTEC — ALTEC AT SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V462000·2026-07-17

    Turtle Top Recalls 2026 Terra Ford Transit Buses Due to Lift Control Failure

    Turtle Top is recalling 2026 Terra Ford Transit buses because an electrical contactor may fail, preventing the wheelchair lift from stopping. This defect increases the risk of injury.

    Product
    TURTLE TOP — TURTLE TOP TERRA FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V465000·2026-07-17

    Great Dane Recalls 2027 Champion Trailers for Rear Impact Guard Defect

    Great Dane is recalling 2027 Champion dry van trailers because they may lack required rear impact guard extension channels, increasing injury risk in crashes.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V464000·2026-07-17

    Foretravel Recalls 2027 Realm Motorcoaches Due to Fire Risk

    Foretravel is recalling 2027 Realm Presidential Motorcoaches because a fan assembly circuit board may overheat, increasing the risk of a fire.

    Product
    FORETRAVEL — FORETRAVEL REALM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26C004000·2026-07-17

    Evenflo Recalls Reo by Revolve360 Child Seats for Headrest Shift Risk

    Evenflo is recalling specific Reo by Revolve360 child seats because the headrest may shift during a crash, increasing injury risk.

    Product
    CHILD SEAT:SHELL:HEADREST:LOCKING MECHANISM recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V460000·2026-07-16

    IC Bus EVSB and CESB school buses recalled for structural body joint defects

    International Motors, LLC is recalling certain 2025-2027 IC Bus EVSB and CESB school buses due to insufficient epoxy coverage on body joints. This defect may cause panels to separate during a crash.

    Product
    IC BUS — IC BUS CESB, EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26628·2026-07-16

    SDADI Kitchen Step Stools Recalled for Entrapment and Fall Hazards

    SDADI Kitchen Step Stools, models LT01 and LT05, can collapse or tip over and allow children's bodies to fit through openings, creating serious injury and death risks. Consumers should stop using them immediately and contact the importer for a refund.

    Product
    SDADI Kitchen Step Stools, models LT01 and LT05
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26617·2026-07-16

    Oitnlaughter LED Finger Lights Recalled for Battery Ingestion Risk

    Oitnlaughter LED Finger Lights sold on Amazon contain easily accessible button cell batteries that pose a risk of serious injury or death if swallowed by children. Consumers should stop using the toys immediately and contact Delightmi for a refund.

    Product
    Oitnlaughter LED Finger Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26621·2026-07-16

    Nottaway Chandelier Fixtures recalled for electrocution hazard risk

    Currey & Company is recalling about 447 Nottaway chandeliers due to lack of proper electrical grounding, which poses a risk of serious injury or death from electrocution. Consumers should stop using them immediately and contact the company for a free replacement.

    Product
    Nottaway Chandelier Fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide