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.

6876–6900 of 84912

  • HighFDA (Devices)·Z-1938-2025·2025-06-18

    MUSE 5 Cardiovascular Systems Recall Administrator Credential Access

    GE Medical Systems is recalling MUSE 5 Systems due to a vulnerability that could allow unauthorized access to patient data. The MUSE Administrator Account credentials could potentially be used to log into affected systems from the local network and manipulate recorded cardiovascular patient data.

    Product
    MUSE 5 Systems, Model Numbers 2021274-001, 2023032-005, 2027478-001, Large capacity client-server-based computer system that accesses stores and manages cardiovascular information.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0934-2025·2025-06-18

    Instant Milk Tea Powder lacks milk allergen declaration

    R&M Trading LLC is recalling Instant Milk Tea Original Flavor because the label does not declare milk, despite containing whey powder and sodium caseinate, which are milk-derived ingredients.

    Product
    Instant Milk Tea Original Flavor, R&M Refresher brand, B0D71YHZX4, net wt. 1lb. Product is sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D71YHZX4 3-pack ASIN #B0D72BLQRW Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1954-2025·2025-06-18

    Tecfen Medical 2.0mm Crescent Knife Ophthalmic Device Recall

    Tecfen Medical is recalling 2.0mm Crescent Knife ophthalmic surgical instruments (Model QKN1010, Lot ZGY24071501-03) due to sterility assurance concerns. The affected devices were distributed in the US and internationally.

    Product
    Brand Name: Tecfen Medical Product Name: 2.0mm Crescent Knife Angled Bevel Up Model/Catalog Number: QKN1010 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile and packaged individually in Tyhvek 1059B. The crescent kn
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1970-2025·2025-06-18

    Alaris Pump Infusion Sets may leak at male luer connections

    BD Switzerland is recalling multiple Alaris Pump Infusion Set models worldwide due to potential leaks at the connection between the closed male luer component and needle-free connector, which could delay procedures, interrupt treatment, expose patients to hazardous drugs, or result in underdosing.

    Product
    Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite Y-Sites, REF: 10013361T; SmartSite Bag Access Non-Vented Bonded Texium Closed Male Luer With Priming Cap, REF: 10321213T; SmartSite Bag Access Non-Vented Low
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1939-2025·2025-06-18

    Femoral Nail T2 GTN Left and Right Versions Mislabeled

    Stryker GmbH is recalling certain Femoral Nail T2 GTN devices because some labeled as left version contained right nails, and vice versa. This mislabeling could result in incorrect surgical implantation.

    Product
    Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1933-2025·2025-06-18

    Philips Intera 1.5T MRI Systems Gradient Coil Fire Risk Recall

    Philips is recalling two Intera 1.5T MRI systems due to a gradient coil component failure that can produce smoke or fire, posing risks of inhalation injury, burns, asphyxia, or death.

    Product
    Intera 1.5T Master/Nova Product Number: 781106;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1947-2025·2025-06-18

    Thermo SCIENTIFIC Sensititre Mueller-Hinton Broth diagnostic device recalled

    Remel, Inc. is recalling one lot of Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth due to off-color that may affect performance of this in-vitro diagnostic device.

    Product
    Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; invitro diagnostic device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0461-2025·2025-06-18

    Chlorthalidone Tablets Recalled Due to Failed Dissolution Specifications

    AvKARE is recalling Chlorthalidone Tablets USP 25 mg due to failed dissolution specifications. The defect may affect the drug's therapeutic effectiveness.

    Product
    CHLORTHALIDONE — CHLORTHALIDONE (CHLORTHALIDONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0469-2025·2025-06-18

    Cephalexin Oral Suspension Recalled for Failed Impurities Specifications

    Ascend Laboratories is recalling Cephalexin for Oral Suspension due to an out-of-specification result in impurity testing that identified Cephalexin Glucose Adduct during stability analysis.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0497-2025·2025-06-18

    Icosapent Ethyl Capsules Recalled for Failed Tablet Specifications

    Zydus Pharmaceuticals is recalling Icosapent Ethyl Capsules due to burnt or melted capsules caused by oxidation from leakage of capsule contents. The recall affects 11,616 bottles distributed in Illinois, Pennsylvania, and Mississippi.

    Product
    ICOSAPENT ETHYL — ICOSAPENT ETHYL (ICOSAPENT ETHYL)
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1937-2025·2025-06-18

    BD BBL CultureSwab EZ Collection and Transport System Swabs Breakage

    BD BBL CultureSwab EZ Collection and Transport System (REF 220144) is being recalled because swabs may break during use. The recall affects units distributed nationwide in Maryland.

    Product
    BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1926-2025·2025-06-18

    DxI 9000 Access Immunoassay Analyzer software version 1.20 recall

    Beckman Coulter is recalling certain DxI 9000 Access Immunoassay Analyzers due to incorrect motor/encoder and cable installation that causes error codes, prevents assays from running, and delays result generation.

    Product
    DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software versions 1.20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1968-2025·2025-06-18

    Guardian System 2 Controller units recalled for battery alert display defect

    Turncare has recalled certain Guardian 2 System controllers because a software issue prevented "low" and "terminal" battery alerts from displaying on the screen in specific circumstances when the device was not running patient therapy.

    Product
    Brand Name: Guardian 2 System Product Name: Guardian System 2 Controller Model/Catalog Number: GS-2.5-C Software Version: 2.5.4-69 (Fix)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0468-2025·2025-06-18

    Cephalexin Oral Suspension Recalled for Failed Impurity Specifications

    Ascend Laboratories is recalling Cephalexin for Oral Suspension due to failed impurity specifications identified during stability testing. An out-of-specification result for Cephalexin Glucose Adduct was observed at six months.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1967-2025·2025-06-18

    Guardian System 2 Controller Software Battery Alert Display Issue

    Turncare is recalling Guardian System 2 Controllers due to a software issue where low and terminal battery alerts do not display on the screen in certain circumstances when the device is not running patient therapy.

    Product
    Brand Name: Guardian 2 System Product Name: Guardian System 2 Controller Model/Catalog Number: GS-2.5-C Software Version: 2.5.4-59 (Fix)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0932-2025·2025-06-18

    Instant Milk Tea Taro Flavor Recalled for Undeclared Milk Allergen

    R&M Refresher brand Instant Milk Tea Powder in Taro Flavor is recalled nationwide because the label does not declare milk, though the product contains Whey Powder and Sodium Caseinate derived from milk.

    Product
    Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLBH, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D72CMLBH 3-pack ASIN #B0D72D6589 Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder,
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1964-2025·2025-06-18

    Baxter Novum IQ Syringe Pump Design Issue Recall

    Baxter is recalling certain Novum IQ Syringe Pumps manufactured or repaired after July 4, 2023, due to a design issue that may falsely detect a syringe flange when none is loaded, causing the pump interface to become stuck or display a System Error 21502.

    Product
    Baxter Novum IQ Syringe Pump, product code 40800BAXUS,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0933-2025·2025-06-18

    Instant Milk Tea Matcha Flavor recalled for undeclared milk allergen

    R&M Refresher Instant Milk Tea Matcha Flavor is recalled because its label declares "Non-Dairy Creamer" but does not specify that the product contains milk (whey powder and sodium caseinate). The product may cause allergic reactions in consumers with milk allergies.

    Product
    Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y85TG, net wt. 1lb. Product was sold in 1-pack or 3-pack. Parent ASIN #B0D728CZWS 1-pack ASIN #B0D71Y85TG 3-pack ASIN #B0D71YBV1X Label declares Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder,
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0462-2025·2025-06-18

    Ezetimibe and Simvastatin Tablets Recalled for Failed Impurity Specifications

    Glenmark Pharmaceuticals Inc., USA is recalling Ezetimibe and Simvastatin Tablets (10mg/40mg) due to out-of-specification results for related substances in a stability study. The recall affects approximately 6,759 bottles distributed nationwide.

    Product
    EZETIMIBE AND SIMVASTATIN — EZETIMIBE AND SIMVASTATIN (EZETIMIBE AND SIMVASTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0470-2025·2025-06-18

    Levothyroxine Sodium tablets recalled for foreign substance contamination

    Macleods Pharmaceuticals is recalling Levothyroxine Sodium 112 mcg tablets (Lot #MLF2401A, expiration 01/31/2026) distributed nationwide due to black hair found embedded in tablets.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0936-2025·2025-06-18

    NOW Nutritional Yeast Powder recalled due to packaging error

    NOW Foods is recalling NOW Nutritional Yeast Powder (10 oz, UPC 7 33739 02460 2) because regular yeast was inadvertently packaged as nutritional yeast.

    Product
    NOW Nutritional Yeast Powder, Nt. Wt. 10oz. UPC 7 33739 02460 2
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V401000·2025-06-13

    Ford Super Duty brake pushrod springs missing; owners told not to drive

    Ford is recalling certain 2025 Super Duty trucks because the brake booster pushrod retaining spring may not have been installed, risking sudden loss of brake function.

    Product
    FORD — FORD F-250 SD, F-350 SD, F-450 SD, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide