The Recall Desk

State

Pennsylvania product recalls

72,936 recalls have nationwide distribution and so reach Pennsylvania. 11,918 additional recalls listed Pennsylvania specifically in their distribution scope.

What the numbers show

Total
11,918
Critical
1,922
Severe
2,866
Most recent
2026-09-09

Of the 11,918 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 2,866 (24%) are Severe.

These figures cover only the 11,918 recalls whose distribution notice names Pennsylvania specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2876–2900 of 84854

  • SevereCPSC·26348·2026-03-26

    FUNTOK ride-on truck circuit boards can overheat and ignite

    FUNTOK 24V 2-Seater Ride-On Trucks are being recalled because the circuit board can overheat and ignite. Eleven reports of fires, sparking, burning, melting and smoking have been received.

    Product
    FUNTOK 24V 2-Seater Ride-On Trucks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V194000·2026-03-26

    Honda CB1000SP fuel feed hose may disconnect causing a fuel leak

    Honda is recalling certain 2025 CB1000SP motorcycles because the fuel feed hose may disconnect from the fuel tank, causing a fuel leak near the rear tire.

    Product
    HONDA — HONDA CB1000SP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E014000·2026-03-26

    Chrysler Recalls Mopar Side Curtain Air Bags for Seam Defect

    Chrysler is recalling specific Mopar side curtain air bags because improperly sealed seams may cause insufficient pressure retention, increasing the risk of ejection and injury during a crash.

    Product
    AIR BAGS:SIDE/WINDOW:CURTAIN recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26342·2026-03-26

    AirClub convertible bassinets create an opening between sleeper and mattress

    AirClub convertible bassinets are being recalled because the mechanism used to attach the product to an adult bed creates an opening between the bedside sleeper and the mattress, posing a fall hazard to infants.

    Product
    AirClub Convertible Bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26344·2026-03-26

    Sunnyyes LED mini lights let children access lithium coin batteries

    Sunnyyes LED mini lights are being recalled because the lithium coin batteries can be easily accessed by children, the remote battery compartment screw does not stay attached, and the packaging lacks required warnings.

    Product
    Sunnyyes LED Mini Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26345·2026-03-26

    GLMZZ fidget magnet balls are high-powered magnets posing ingestion hazard

    GLMZZ Fidget Magnet Ball Toy Sets are being recalled because they are high-powered magnets, violating the mandatory standard for toys and posing an ingestion hazard to children.

    Product
    GLMZZ Fidget Magnet Ball Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26347·2026-03-26

    Petzl Nomic and Ergonomic ice axe shafts can break at handle

    Petzl America is recalling Nomic and Ergonomic ice climbing axes because the shaft can break at the handle during use. Twenty-six shaft breakages have been reported, with no injuries.

    Product
    Nomic and Ergonomic Ice Climbing Axes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26349·2026-03-26

    DIY sauna heater kit conductors can overheat posing a fire hazard

    Plunge Buddy is recalling DIY Sauna Heater Kits because electrical conductors within the kits can overheat. Twelve reports of overheating have been received, with no fires or injuries.

    Product
    DIY Sauna Heater Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26346·2026-03-26

    CCCEI power strips lack supplementary overcurrent protection posing fire risk

    CCCEI power strips are being recalled because they do not contain supplementary overcurrent protection, creating a fire risk if overloaded. Two reports of sparking and melting have been received.

    Product
    CCCEI Power Strips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26350·2026-03-26

    MPINOI adult portable bed rails pose entrapment and asphyxiation hazard

    MPINOI adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and mattress, and the rails lack the required hazard warning labels.

    Product
    MPINOI Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V189000·2026-03-26

    Chrysler Voyager and Pacifica side curtain airbags recall

    Chrysler is recalling certain 2022–2026 Voyager and Pacifica vehicles because the right and left side curtain airbags may have insufficient pressure retention due to improperly sealed seams, increasing the risk of ejection and injury during a crash.

    Product
    CHRYSLER — CHRYSLER PACIFICA, VOYAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V191000·2026-03-26

    ABC Bus Recalls Van Hool Buses Due to Incorrect Window Glazing

    ABC Bus is recalling specific Van Hool bus models because the front entrance door window may have incorrect glazing, which could reduce driver visibility and increase crash risk.

    Product
    VAN HOOL — VAN HOOL CX45, TX45, C2045, T2145
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V186000·2026-03-25

    2025-2026 Volvo VNL Trucks Delayed Service Brake Release Recall

    Volvo Trucks is recalling certain 2025-2026 VNL (4) vehicles because the service brake may take longer than expected to release, creating a crash risk and violating Federal Motor Vehicle Safety Standard 121.

    Product
    VOLVO — VOLVO VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0528-2026·2026-03-25

    Webcol alcohol prep pads recalled as Class I for microbial contamination

    Cardinal Health is recalling Webcol Alcohol Prep pads because of non-sterility, with microbial contamination identified as Paenibacillus phoenicis. The FDA has classified this recall as Class I.

    Product
    Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive, Waukegan, IL 60085.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V184000·2026-03-25

    2026 Volvo VNL Trucks Instrument Panel May Fail While Driving

    Volvo Trucks is recalling certain 2025–2026 VNL (4) vehicles because the instrument panel may fail while driving, potentially hiding critical safety information like the speedometer and warning lights.

    Product
    VOLVO — VOLVO VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1570-2026·2026-03-25

    GE Centricity Viewer 6.0 may expose login credentials on workstations

    GE Medical Systems is recalling Centricity Universal Viewer software versions 6.0 through 6.0 SP10.4.1 because user login credentials may be exposed on the local client workstation.

    Product
    Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 210
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1571-2026·2026-03-25

    GE Centricity Viewer 5.0 may expose login credentials on workstations

    GE Medical Systems is recalling Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 because user login credentials may be exposed on the local client workstation.

    Product
    Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1582-2026·2026-03-25

    ConvaTec EsteemBody drainable pouch REF 423643 may leak

    ConvaTec is recalling two lots of the EsteemBody Drainable Pouch, REF 423643, because the drainable large pouch may leak due to a manufacturing issue.

    Product
    Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1573-2026·2026-03-25

    Welch Allyn vision screener display may flicker inducing photosensitive seizures

    Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.

    Product
    Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit pe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0585-2026·2026-03-25

    Wawa Reduced Fat Milk 2% Recalled for Foreign Plastic Material

    Wawa Beverage Company is recalling Wawa Reduced Fat Milk 2% 16 oz containers because foreign plastic material was discovered on the fill line during production.

    Product
    Wawa Reduced Fat Milk 2% 16 oz (Pint)
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1572-2026·2026-03-25

    Stryker sagittal saw attachment cover screws may loosen and detach

    Howmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment because the external screws securing the cover to the saw housing may loosen and detach during use.

    Product
    MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1586-2026·2026-03-25

    Hologic Aptima HPV assay may produce invalid or false negative results

    Hologic is recalling one master lot of the Aptima HPV Assay because the product exhibits potential to generate either invalid or false negative results.

    Product
    Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide