The Recall Desk

State

Pennsylvania product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4076–4100 of 84858

  • ModerateFDA (Drugs)·D-0231-2026·2025-12-24

    Mepivacaine dental cartridges recalled over cracked and broken containers

    Novocol Pharmaceutical of Canada is recalling 5,520 cartons of Mepivacaine HCl 3% injection over a defective container with cracked or broken cartridges.

    Product
    MEPIVACAINE — MEPIVACAINE (MEPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0945-2026·2025-12-24

    Gluteal implants recalled over specification deviations and missing premarket clearance

    DSAART is recalling 118 AART Gluteal Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.

    Product
    Brand Name: AART Gluteal Implant Product Name: Gluteal Implant Model/Catalog Numbers: 501-101 - Gluteal Implant style 1 size 1 UDI-DI code: B490501101 501-103 - Gluteal Implant style 1 size 3 UDI-DI code: B490501103 501-101 UDI-DI code: B490501101 501-103 - Gluteal
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-0946-2026·2025-12-24

    Chin implants recalled over specification deviations and missing premarket clearance

    DSAART is recalling 29 AART Chin Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.

    Product
    Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog Numbers: 400-0101 Chin Implant style 1 size 1 UDI-DI code: B490400101 400-0103 Chin Implant style 1 size 3 UDI-DI code: B490400103 400-0104 Chin Implant style 1 size 4 UDI-DI code: B490400104 40
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Drugs)·D-0228-2026·2025-12-24

    Xylocaine dental cartridges recalled over cracked and broken containers

    Novocol Pharmaceutical of Canada is recalling 18,789 cartons of 2% Xylocaine Dental with Epinephrine over a defective container with cracked or broken cartridges.

    Product
    2% Xylocaine DENTAL with Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose cartridges, 1.7 mL each, Rx only, Manufactured for Dentsply Pharmaceutical, York, PA 17404, by Novocol Pharmaceutical of Canada, Inc., NDC
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0948-2026·2025-12-24

    Pectoral implants recalled over specification deviations and missing premarket clearance

    DSAART is recalling 41 AART Pectoral Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.

    Product
    Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/Catalog Number: 500-106-5 Pectoral Implant style 1 size 6 left UDI-DI code: B4905001065 500-106-6 Pectoral Implant style 1 size 6 right UDI-DI code: B4905001066 500-200-5 Pectoral Implant style 2 si
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-0947-2026·2025-12-24

    Malar facial implants recalled over specification deviations and missing clearance

    DSAART is recalling 2 AART Malar Implants because the products deviated from established specifications and were distributed without the required FDA premarket approvals or clearances.

    Product
    Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog Number: 401-202-5 Malar Implant style 2 size 2 left UDI-DI code: B4904012025 401-202-6 Malar Implant style 2 size 2 right UDI-DI code: B4904012026
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Drugs)·D-0240-2026·2025-12-24

    Ciclopirox shampoo recalled after failing impurity specifications at eighteen months

    Sun Pharma/Taro is recalling 17,664 units of Ciclopirox Shampoo 1% after out of specification impurity and degradation results at the 18-month timepoint.

    Product
    Ciclopirox Shampoo, 1%, 120 mL, Rx only, Mfg by: Taro Pharmaceuticals Inc., Ontario, Canada; Dist. by: Taro Pharmaceuticals USA, Inc., NY 10532. NDC 51672-1351-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0943-2026·2025-12-24

    Respiratory specimen reagent recalled because fluidification cannot be guaranteed

    Copan Italia is recalling 122,850 units of 1ml DTT liquid reagent because treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.

    Product
    1ml of DTT in liquid phase, in PET tube with capture cap, in bulk
    Category
    Medical Device
    Distribution
    14 states
  • SevereNHTSA·25V909000·2025-12-23

    Altec Recalls 2022-2023 Aerial Work Platforms Due to Missing Check Valve

    Altec is recalling 2022-2023 AA55, AM55, AN46, and AN55 vehicles because a missing check valve may reduce boom insulation, increasing the risk of electric shock.

    Product
    ALTEC — ALTEC AN46, AM55, AA55, AN55
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V907000·2025-12-23

    KTM motorcycle side stand spring may break and fall down

    KTM is recalling certain 2025 390 Adventure R, 390 Adventure X, 390 SMC R and 390 Enduro R motorcycles because engine vibrations may break the side stand spring, letting the stand fall to the ground.

    Product
    KTM — KTM 390 ENDURO R, 390 ADVENTURE X, 390 SMC R, 390 ADVENTURE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V906000·2025-12-23

    BMW i4 positive battery cable connection may become loose

    BMW is recalling one 2025 i4 eDrive40 vehicle because the connection between the positive battery cable and the rear power distributor may become loose.

    Product
    BMW — BMW I4 EDRIVE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V911000·2025-12-23

    Honda CBR650R wiring damage can blow the fuse for lights

    Honda is recalling certain 2024-2025 CBR650R motorcycles because engine vibration may damage the turn signal switch wire harness, causing a short circuit and a blown fuse.

    Product
    HONDA — HONDA CBR650R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V908000·2025-12-23

    Volvo rearview camera image may not display when reversing

    Volvo is recalling certain 2021-2025 vehicles across the XC40, XC60, XC90, S60, S90, V60 and V90 ranges because the rearview camera image may not display when the vehicle is in reverse.

    Product
    VOLVO — VOLVO XC90, XC60, V90CC, XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V910000·2025-12-23

    Spartan Fire Emergency Vehicles Recalled for Ladder Handle Defect

    Spartan Fire is recalling certain emergency vehicles because a ladder handle may detach, allowing ground ladders to fall off and creating a road hazard.

    Product
    SPARTAN FIRE — SPARTAN FIRE STAR SERIES, UST BODY, LEGEND SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V905000·2025-12-23

    Tiffin motorhome generator wiring harness may contain undersized wires

    Tiffin is recalling certain 2025-2026 Open Trail motorhomes fitted with an optional diesel or propane generator because the wiring harness may contain incorrectly sized wires.

    Product
    TIFFIN — TIFFIN OPEN TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V912000·2025-12-23

    2026 Nissan Rogue Vehicles with Incorrect Spare Tire Assembly

    Nissan is recalling 2026 Rogue vehicles with an incorrect-size spare tire that does not match the tire placard information. This may lead to improper tire inflation and increased crash risk.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E092000·2025-12-22

    Couture Co Recalls Specific Volt E-Bike Carriers Due to Latch Wear

    Couture Co is recalling four models of Volt e-bike carriers because the latch mechanism may wear excessively and disengage while driving.

    Product
    EQUIPMENT:MECHANICAL:CARRIER/RACK recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V899000·2025-12-19

    Audi automatic locking retractor may not engage for child seats

    Volkswagen is recalling certain 2025 Audi models because the automatic locking retractor may fail to engage when a child seat is installed using the seat belt.

    Product
    AUDI — AUDI S5, Q6 E-TRON, A5, A6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·041-2025·2025-12-19

    Olympia Provisions Recalls Holiday Kielbasa Sausage Due to Metal Contamination

    Olympia Provisions is recalling approximately 1,930 pounds of ready-to-eat holiday kielbasa sausages that may contain metal. The recall covers products sold in California, Oregon, and Washington, as well as nationwide online sales.

    Product
    Olympia Provisions — Olympia Provisions Recalls Ready-to-Eat Holiday Kielbasa Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V895000·2025-12-19

    Coach and Equipment Recalls 2024-2025 Phoenix Transit Buses Due to Fire Risk

    Coach and Equipment is recalling 2024-2025 Phoenix transit buses with propane conversion kits because the alternator may damage the fuel line, increasing fire risk.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX
    Category
    Vehicle
    Distribution
    Distributed nationwide