The Recall Desk

State

Pennsylvania product recalls

72,969 recalls have nationwide distribution and so reach Pennsylvania. 11,919 additional recalls listed Pennsylvania specifically in their distribution scope.

What the numbers show

Total
11,919
Critical
1,922
Severe
2,866
Most recent
2026-09-16

Of the 11,919 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 11,919 recalls whose distribution notice names Pennsylvania specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4751–4775 of 84888

  • HighFDA (Food)·H-0158-2026·2025-11-12

    Cooked peeled tail off shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 3,600 cases of Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp because the shrimp may be contaminated with Cesium-137.

    Product
    Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp, net wt. 2lbs. UPC 011110626196. Product is packaged in clear plastic bag and has a white label with green stripes on top of each bag.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0426-2026·2025-11-12

    Straight extension catheter trays recalled over header bag seal integrity

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions, 12 Fr x 24 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Safety Components: 12 Fr/Ch (4.0 mm) x 24 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0164-2026·2025-11-12

    Extra large peeled shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 1,458 cases of Publix Extra Large Shrimp Easy to Peel Deveined 21/25 because the shrimp may be contaminated with Cesium-137.

    Product
    Publix Extra Large Shrimp Easy to Peel Deveined 21/25, net wt. 1.5 lbs. UPC 041415064454. Product was sold at Publix.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0425-2026·2025-11-12

    Straight extension catheter trays 24 cm recalled over header bag seals

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions and IC components, 12 Fr x 24 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 24 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V776000·2025-11-12

    Winnebago Recalls 2025-2026 Micro Minnie Travel Trailers Due to Fire Risk

    Winnebago is recalling 2025-2026 Micro Minnie travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire risk.

    Product
    WINNEBAGO — WINNEBAGO MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0162-2026·2025-11-12

    Frozen raw white shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 7,200 cases of AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, sold at WinCo, because the shrimp may be contaminated with Cesium-137.

    Product
    AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, net wt. 5 lbs. UPC 731149654075. Product was sold at WinCo.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0424-2026·2025-11-12

    Twenty centimetre straight catheter trays recalled over header bag seal integrity

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions, 12 Fr x 20 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0152-2026·2025-11-12

    Clomipramine 25 mg capsules recalled over nitrosamine above the intake limit

    Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 25 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0153-2026·2025-11-12

    Clomipramine 50 mg capsules recalled over nitrosamine above the intake limit

    Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 50 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0154-2026·2025-11-12

    Clomipramine 75 mg capsules recalled over nitrosamine above the intake limit

    Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 75 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0435-2026·2025-11-12

    Flex Focus ultrasound carts recalled over incomplete battery safety instructions

    B-K Medical is recalling 4,426 1202 Flex Focus ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    1202 Flex Focus Ultrasound System, cart models UA1214 and UA1814, used with: Flex Focus 200, Flex Focus 300, Flex Focus 400, Flex Focus 500, Flex Focus 700, Flex Focus 800; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0438-2026·2025-11-12

    bk3000 ultrasound systems recalled over incomplete battery replacement guidance

    B-K Medical is recalling 496 bk3000 ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    bk3000 Ultrasound System w/battery; Model No. 2300-66; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0440-2026·2025-11-12

    Ultrasound systems recalled over battery guidance missing from the manuals

    B-K Medical is recalling 895 bk5000 ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    bk5000 Ultrasound System w/battery; Model No. 2300-61; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0439-2026·2025-11-12

    bk3500 ultrasound systems recalled over incomplete battery safety instructions

    B-K Medical is recalling 124 bk3500 ultrasound systems because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    bk3500 Ultrasound System w/battery; Model No. 2300-41; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0437-2026·2025-11-12

    bkActiv ultrasound systems recalled over battery guidance missing from manuals

    B-K Medical is recalling 567 Ultrasound System 2300 bkActiv units because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    UUltrasound System 2300, bkActiv w/battery; Model No. 2300-11; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0436-2026·2025-11-12

    bkSpecto ultrasound systems recalled over battery guidance gaps in manuals

    B-K Medical is recalling 1,697 Ultrasound System 1300 bkSpecto units because the user guide and service manual do not adequately state battery replacement intervals, end-of-life handling or safety precautions.

    Product
    Ultrasound System 1300, bkSpecto w/battery; Model No. 1300-21 or 1300-S1; System, Imaging, Pulsed Doppler, Ultrasonic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V773000·2025-11-10

    Nova Bus Recalls 2024-2025 LFS Transit Buses for Seat Belt Defect

    Nova Bus is recalling 2024-2025 LFS transit buses because the driver's seat belt may be pinched by the partition, preventing proper retraction and increasing injury risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E074000·2025-11-07

    AROW Emergency Exit Window Latch Failure Recall

    AROW Global Corp is recalling emergency exit windows because the latch can fail during a crash, increasing the risk of passenger injury.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V768000·2025-11-06

    GM Recalls 2019-2020 Chevrolet Silverado Medium Duty Trucks for Brake Wiring Defect

    General Motors is recalling 2019-2020 Chevrolet Silverado 4500, 5500, and 6500 trucks because a brake jumper wire harness may lack protective tape, risking power brake assist failure.

    Product
    CHEVROLET — CHEVROLET SILVERADO 6500, SILVERADO 5500, SILVERADO 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide