The Recall Desk

State

Pennsylvania product recalls

72,992 recalls have nationwide distribution and so reach Pennsylvania. 11,920 additional recalls listed Pennsylvania specifically in their distribution scope.

What the numbers show

Total
11,920
Critical
1,922
Severe
2,867
Most recent
2026-09-25

Of the 11,920 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 2,867 (24%) are Severe.

These figures cover only the 11,920 recalls whose distribution notice names Pennsylvania specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7151–7175 of 84912

  • HighCPSC·25291·2025-05-22

    Holiday Lane Infant Footed Pajamas Recalled for Ankle Elastic Injury Hazard

    Macy's is recalling Holiday Lane Infant Footed Pajamas because the ankle elastic can be too tight, restricting blood circulation and causing injury. The company has received four reports of chafing, imprinting, or circulation restriction.

    Product
    Holiday Lane Infant Footed Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V335000·2025-05-22

    Shyft Recalls 2022-2024 Utilimaster Velocity Vehicles Missing Tire Placards

    Shyft Group is recalling 2022-2024 Utilimaster Velocity vehicles because they may be missing the tire and information placard, which is required by federal safety standards.

    Product
    UTILIMASTER — UTILIMASTER VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E037000·2025-05-22

    Zoox Recalls Driverless Vehicles for Software Defect in Person Detection

    Zoox is recalling Automated Driving Systems with older software that may fail to detect people next to the vehicle, increasing injury risk.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-05222025-01·2025-05-22

    USDA Issues Alert for Chicken Soup with Undeclared Wheat Allergen

    USDA FSIS issued a public health alert for Signature SELECT chicken soup cups containing undeclared wheat. Consumers with wheat allergies should not consume the products.

    Product
    FSIS Issues Public Health Alert for Chicken Soup Product Due To Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1727-2025·2025-05-21

    iGo2 DC Car Adapter Recall: Overheating and Housing Deformation Risk

    Medical Depot Inc. is recalling 89,532 units of the iGo2 DC Car Adapter used with iGo2 Portable Oxygen Concentrator Systems. The DC power supply housing may become excessively hot to the touch and deform, posing a burn and fire hazard.

    Product
    iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0768-2025·2025-05-21

    Bonya Lemon Yogurt Parfait Recalled for Undeclared Almonds

    Knockroe Inc is recalling Bonya Lemon Yogurt Parfait (8oz) because it contains undeclared almonds, a common allergen. The product was distributed to New York, Pennsylvania, Massachusetts, and New Jersey.

    Product
    Bonya Lemon Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0763-2025·2025-05-21

    Bonya Strawberry Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Strawberry Yogurt Parfait cups (8 oz) distributed to NY, PA, MA, and NJ because they contain undeclared almonds, a common allergen.

    Product
    Bonya Strawberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0772-2025·2025-05-21

    Bonya Passion Fruit Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Passion Fruit Yogurt Parfait (8 oz) due to undeclared almonds, which poses a risk to consumers with tree nut allergies. The product was distributed to New York, Pennsylvania, Massachusetts, and New Jersey.

    Product
    Bonya Passion Fruit Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0774-2025·2025-05-21

    Bonya Black Cherry Yogurt Parfait Recalled for Undeclared Almonds

    Knockroe Inc is recalling Bonya Black Cherry Yogurt Parfait due to undeclared almonds, which pose a risk to people with tree nut allergies. The product was distributed in NY, PA, MA, and NJ.

    Product
    Bonya Black Cherry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0776-2025·2025-05-21

    Tomatoes Recall Due to Potential Salmonella Contamination

    Ray & Mascari, Inc. is recalling tomatoes sold in retail 4-count clam shell containers and bulk cardboard cases due to potential Salmonella contamination. Affected products were distributed in IN, KY, MA, MD, MI, NC, OH, PA, and WI.

    Product
    Tomatoes, retail 4 Count Vine Ripe Tomatoes packaged in clam shell containers [20 oz. (1 lb. 4 oz) 567g] with UPC# 7 96553 20062 1; 12 retail clam shells per case. Bulk 25# 6x6 tomatoes (cardboard case), bulk 10# 6x6 Tomatoes (cardboard case), bulk 25# Random #2 Tomatoes (cardbo
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-1763-2025·2025-05-21

    LifeShield Infusion Safety Software Recalled for Drug Library Defects

    ICU Medical is recalling LifeShield Drug Library Management software v2.1 and v2.2 due to defects that could allow over-delivery of medication to patients or unauthorized modification of drug parameters.

    Product
    LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0773-2025·2025-05-21

    Bonya Strawberry-Banana Yogurt Parfait Recalled Due to Undeclared Almonds

    Knockroe Inc is recalling Bonya Strawberry-Banana Yogurt Parfait (8oz) because the product contains undeclared almonds, which pose a risk to consumers with tree nut allergies.

    Product
    Bonya Strawberry-Banana Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0770-2025·2025-05-21

    Bonya Pineapple Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Pineapple Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ because the product contains undeclared almonds, a common allergen that is not listed on the label.

    Product
    Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0420-2025·2025-05-21

    Testosterone Cypionate Injection 200 mg/mL Recalled for Sterility Assurance

    Empower Pharmacy is recalling Testosterone Cypionate Injection 200 mg/mL (Lot 202364, 8,230 vials) distributed nationwide because the manufacturer cannot assure the product's sterility. Consumers should stop using the product and consult their healthcare provider.

    Product
    Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only, 5 mL Sterile Multiple-Dose Vial, Compounded by: Empower Pharmacy, 7601 N Sam Houston Pkwy W Ste 100, Houston, TX, 77064, Phone: (877) 562-8577, Compounding Date: 08/20/2024, Beyond Use by Date: 05/28/2025, Lot 202364.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1698-2025·2025-05-21

    AirLife Infant Heated Wire Circuit Adapter Disconnection Risk Recall

    Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (model AH265) because adapters may disconnect during setup or use, potentially interrupting ventilation to newborns. Disconnection can cause hypoxia, hypercapnia, and organ failure.

    Product
    Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH265 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit Kit Dual-limb, Dual-heat, high-flow circuit (>4 L/min) Contains AH165 Circuit, AH290 Chamber Compone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1730-2025·2025-05-21

    MedicaLyte Liquid Bicarbonate Concentrate Recalled for Foreign Matter

    Nipro Renal Solutions USA is recalling MedicaLyte Liquid Bicarbonate Concentrate (models BC+201 and BC+100) due to the potential presence of visible foreign matter in the product.

    Product
    MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in corrugated shipper cases (4 bottles per shipper case).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1697-2025·2025-05-21

    AirLife Infant Heated Wire Circuit Adapter Disconnection Risk

    Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (Model AH165) because adapters may disconnect during setup or use, interrupting ventilation to infants and potentially causing severe complications.

    Product
    Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH165 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit dual-limb, dual-heat, high-flow circuit (>4 L/min) Component: No. a conduit for respiratory gas bet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1750-2025·2025-05-21

    TufTex Over-the-Wire Embolectomy Catheter incomplete sterile barrier

    LeMaitre Vascular is recalling TufTex Over-the-Wire Embolectomy Catheters due to incomplete seals on some packages that compromise the sterile barrier. Affected units were distributed nationwide and internationally.

    Product
    TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34, 1651-38, 1651-44, 1651-48, 1651-58, 1651-64, 1651-68, 1651-78, 1651-84, 1651-88, E1651-34, E1651-38, E1651-44, E1651-48, E1651-64, E1651-68, E1651-78, E1651-84, E1651-88, 1651-44J, 1651-48J, 1651-84J, 1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1769-2025·2025-05-21

    KliniTray Platte Faxitron Sterile Tissue Resection Examination Board Recalled

    KliniTray Platte Faxitron sterile tissue resection margin examination boards (Model 2001155-F) are being recalled due to potential for microbial contamination. Affected units were distributed nationwide.

    Product
    KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1752-2025·2025-05-21

    Pruitt Irrigation Occlusion Catheter Recalled for Incomplete Sterile Seals

    LeMaitre Vascular is recalling Pruitt Irrigation Occlusion Catheters (Catalog Numbers 2102-09, E2102-09) due to incomplete sterile barrier seals found during internal testing. The defect affects approximately 26,872 units distributed nationwide and internationally.

    Product
    Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0767-2025·2025-05-21

    Bonya Peach Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Peach Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ due to undeclared almonds that may pose a risk to consumers with tree nut allergies.

    Product
    Bonya Peach Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0765-2025·2025-05-21

    Bonya Blueberry Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Blueberry Yogurt Parfait (8 oz) distributed in NY, PA, MA, and NJ because the product contains undeclared almonds, which poses a risk to consumers with tree nut allergies.

    Product
    Bonya Blueberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0777-2025·2025-05-21

    Kasundi Peeled Mango Pickle in Oil recalled for elevated lead levels

    Advance Food International Inc. is recalling Kasundi Peeled Mango Pickle in Oil due to elevated lead levels detected in the product. The affected product was distributed in the Northeast.

    Product
    National brand Kasundi PEELED MANGO PICKLE IN OIL; Net Wt.: 1 Kg (35.27 oz)/ 2.20lb; Ingredients: Kasundi (Peeled Mango), Canola Oil, Cabbage, Salt, Mixed Spices, Vinegar, Sodium Benzoate as preservative; Product of Pakistan; packaged in a plastic jar with a red lid
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0764-2025·2025-05-21

    Bonya Vanilla Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Vanilla Yogurt Parfait (8oz) due to undeclared almonds, which pose a risk to consumers with almond allergies. The product was distributed to NY, PA, MA, and NJ.

    Product
    Bonya Vanilla Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1766-2025·2025-05-21

    Centurion Sterile Weitlaner Retractor recalled for sterile packaging puncture risk

    Medline Industries is recalling Centurion Sterile Weitlaner Retractor 3 x 4 Prong units because the retractors may puncture through the sterile packaging. The product is distributed nationwide.

    Product
    Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
    Category
    Medical Device
    Distribution
    Distributed nationwide