The Recall Desk

State

Pennsylvania product recalls

20,371 recalls have nationwide distribution and so reach Pennsylvania. 0 additional recalls listed Pennsylvania specifically in their distribution scope.

About recalls in Pennsylvania

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.

16501–16525 of 20371

  • HighFDA (Devices)·Z-1306-2022·2022-07-06

    NaviCare Nurse Call System Cancels Patient Calls During Wireless Use

    The NaviCare Nurse Call system software (versions 3.9.100-3.9.300) has a wireless integration defect causing patient calls to be canceled when answered on wireless phones. The issue affects 283 installations in the US and Canada.

    Product
    NaviCare Nurse Call/Voalte Nurse Call
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1305-2022·2022-07-06

    Laparoscopic irrigator recalled for inability to provide irrigation

    Davol, Inc. is recalling the HydroSurg Plus Laparoscopic Irrigator because the device cannot provide irrigation as intended. The recall affects 4,390 units in the US and 390 in Canada.

    Product
    HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 33cm Tip and Cojoined Suction and Irrigation Tubing, Catalog Number 0026870
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1310-2022·2022-07-06

    FDA Recalls TEG 5000 Fibrinogen Reagent Kits Due to Outdated Reference Ranges

    Haemonetics Corporation is recalling TEG 5000 Functional Fibrinogen Reagent kits because the reference ranges in the instructions have shifted. Clinicians using these outdated ranges could misdiagnose patients or fail to provide necessary treatment.

    Product
    TEG 5000 Functional Fibrinogen Reagent, Item No. 07-034
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1308-2022·2022-07-06

    Surgical Light Paint Particles May Fall Into Operating Field

    Paint particles may detach from VOLISTA StandOP Surgical Lights and fall into the operating field during surgery, risking infection and organ irritation. Getinge Usa Sales Inc is recalling 337 affected units in the United States.

    Product
    VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP ARD568811961 VLT600DF AIM STP ARDVST229000A VST60SF AIM ARDVST229001A VST60DF AIM ARDVST229002A VST66SF AIM ARDVST229003A VST66DF AIM ARDVST229034A VST60SF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1303-2022·2022-07-06

    Fresenius Optiflux 200NRe Dialyzers Recalled Due to Temperature Exposure

    Fresenius Medical Care is recalling 19 cases of Optiflux 200NRe dialyzers distributed in Pennsylvania after exposure to cold temperatures outside safe storage ranges. Affected lot number is 22AU04017.

    Product
    Optiflux 200NRe Dialyzer Finished Assy., Model no. 0500320E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1170-2022·2022-07-06

    Calcipotriene Scalp Solution Recalled Due to Defective Delivery System

    Akorn, Inc. is recalling Calcipotriene Topical Solution 0.005% (Scalp Solution) nationwide due to a defective delivery system that could prevent the product from dispensing properly.

    Product
    Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only, 60 mL (2 fl. oz.) bottle, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, N.Y. 11701. NDC: 50383-732-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1301-2022·2022-07-06

    IVUS Catheter Recall: Missing Contraindications in Instructions

    Volcano Corp is recalling Visions PV. 035 Digital IVUS Catheters because instructions for use do not include contraindications information. Healthcare providers should contact the manufacturer for complete safety documentation before use.

    Product
    Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1288-2022·2022-07-06

    FDA recalls MAC laryngoscope sets due to packaging error

    Baxter Healthcare Corporation is recalling MAC laryngoscope devices due to a packaging error. The recall affects 99 units distributed worldwide.

    Product
    #1 MAC F/O LARYNGOSCOPE; F/O Laryngoscope Set-MAC; F/O Laryngoscope Set-MAC W/LED
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1302-2022·2022-07-06

    Digital IVUS Catheter Recalled for Missing Contraindication Information

    Volcano Corp is recalling 7,520 units of the Volcano Visions PV. 035 Digital IVUS Catheter due to missing contraindication information in the instructions for use. The IFU lacks details about situations where the device should not be used.

    Product
    Volcano Visions PV. 035 Digital IVUS Catheter REF 81234, PN: 300007367341 , Rx Only, Sterile EO, CE 2797
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V369000·2022-07-05

    2021–2022 Heavy-Duty Trucks Recalled for Loose Tie Rod Assembly Components

    Daimler Trucks North America is recalling certain 2021–2022 heavy-duty trucks including Freightliner and Western Star models due to potentially loose tie rod clamps. Loose or detached tie rod ends could cause steering loss and increase crash risk.

    Product
    WESTERN STAR — 2021 WESTERN STAR 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V366000·2022-07-05

    International and IC Bus commercial vehicles recalled for fuel rail assembly defect

    Navistar is recalling certain 2018-2021 International and IC Bus commercial vehicles due to a fuel rail assembly defect. A sealing washer may not seat correctly, allowing fuel leaks that could ignite.

    Product
    INTERNATIONAL — 2021 INTERNATIONAL MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V370000·2022-07-05

    Thomas Built School Buses Recalled for Loose Tie Rod Defect

    Daimler Trucks is recalling 2021-2022 Thomas Built school buses due to loose tie rod clamps that could cause steering failure. Approximately 479 vehicles are affected.

    Product
    THOMAS BUILT BUSES — 2022 THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V227000·2022-07-04

    Western Star commercial trucks recalled for detaching hood air intake covers

    Daimler Trucks North America is recalling certain 2020-2023 Western Star trucks equipped with side air intakes on the hood. The stainless steel cover may loosen and detach, creating a road hazard and increasing crash risk.

    Product
    WESTERN STAR — 2020 WESTERN STAR 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V096000·2022-07-02

    BMW Recalls Multiple 2019-2021 Models for Rearview Camera Software Issues

    BMW is recalling 13,858 vehicles from 2019-2021 model years due to rearview camera software issues that may obscure visibility when reversing. Dealers will update the software free of charge.

    Product
    BMW — 2020 BMW 840I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V065000·2022-07-02

    Roadtrek Recreational Vehicles Recalled for Unattached Propane Lines

    Roadtrek is recalling certain 2021-2022 recreational vehicles because the propane line may not be attached to the water heater. An unattached propane line can allow gas to enter the vehicle, increasing the risk of a fire.

    Product
    ROADTREK — 2021 ROADTREK PLAY SLUMBER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V098000·2022-07-02

    2022 Volvo VNL trucks recalled for wheels that may bend or break

    Volvo Trucks is recalling certain 2022 VNL trucks with Alcoa Mirror Polish Wheels that may fail to support the load, increasing crash risk. Affected wheels will be replaced at no cost by dealers.

    Product
    VOLVO — 2022 VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V004000·2022-07-01

    2022 Forest River Cardinal Trailers Recalled for Tire Belt Separation

    Forest River, Inc. is recalling certain 2021-2022 fifth wheel trailers equipped with defective Sailun tires that may experience belt separation. The defect could cause loss of vehicle control and increase the risk of a crash.

    Product
    FOREST RIVER — 2022 FOREST RIVER CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V003000·2022-07-01

    2022 Forest River Aurora travel trailers recalled for furnace cooktop fire risk

    Forest River is recalling 2021-2022 Aurora and Catalina travel trailers because the panel sealing the cooktop from the furnace was not properly sealed, which could cause an inverted flame and fire risk.

    Product
    FOREST RIVER — 2022 FOREST RIVER AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22177·2022-06-30

    Children's Pajamas Recalled for Flammability Standards Violation

    Kids Tales-branded children's pajamas fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 9,100 units sold online at Amazon from November 2021 through April 2022 are affected.

    Product
    Children's Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22175·2022-06-30

    RIO-Branded Swinging Hammock Chairs Recalled Due to Collapse Injury Hazard

    ShelterLogic Group is recalling approximately 786,000 RIO-branded swinging hammock chairs because improper pin insertion during assembly can cause the chair's legs to collapse, injuring users. The company has received 24 reports of injuries including bruises, lacerations, concussions, and back strain.

    Product
    RIO-branded Swinging Hammock Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22178·2022-06-30

    Children's Nightgowns Recalled for Flammability Standards Violation

    iMOONZZZ children's nightgowns sold on Amazon fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 2,000 units sold between June 2019 and May 2022 are affected.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22176·2022-06-30

    Laars Residential Gas-Fired Boilers Recalled for Carbon Monoxide Risk

    Laars Heating Systems is recalling about 545 residential gas-fired boilers because a malfunctioning blocked vent temperature switch can release carbon monoxide into homes. No injuries have been reported.

    Product
    Residential atmospheric gas-fired boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22754·2022-06-30

    Mohnark Lidocaine 4% Topical Anesthetic Cream Recalled for Non-Child-Resistant Packaging

    Mohnark Pharmaceuticals is recalling Lidocaine 4% Topical Anesthetic Cream because the packaging does not meet child-resistant requirements, creating a poisoning risk if young children ingest the product. About 9,000 units sold online were affected.

    Product
    Lidocaine 4% Topical Anesthetic Cream
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateCPSC·22753·2022-06-30

    Yamaha Kodiak 700 ATVs Recalled for Missing Load Limit Label

    Yamaha is recalling about 3,500 Model Year 2021 and 2022 Kodiak 700 ATVs because they are missing the "Maximum Loading Limit" label, which can result in unsafe trailer towing and crash hazards.

    Product
    Model Year 2021 and 2022 Kodiak 700 All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide