The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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20276–20300 of 114364

  • HighFDA (Devices)·Z-0113-2024·2023-10-25

    Stryker Tornier Reversed Glenoid Baseplate Recalled for Manufacturing Defect

    One lot of Stryker Tornier Perform Reversed Glenoid Baseplate components was manufactured with incorrect 6mm spacers instead of 3mm, preventing proper assembly. The defect affects 30 units distributed across ten US states.

    Product
    stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ502
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-0112-2024·2023-10-25

    Monoject tuberculin syringes incompatible with certain IV connectors

    Cardinal Health is recalling Monoject tuberculin syringes because the conical tip is incompatible with certain needleless IV connectors.

    Product
    Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0056-2024·2023-10-25

    Intraocular Moxifloxacin Injection Recalled Due to Sterility Assurance Issues

    Pine Pharmaceuticals is recalling 2,484 syringes of Moxifloxacin intraocular injection nationwide due to lack of sterility assurance in the compounded product.

    Product
    Moxifloxacin in Balanced Salt Solution, Solution for Intraocular Injection, 600 mcg/0.4mL (150 mcg/0.1mL) Syringe, Rx only, Compounded by: Pine Pharmaceuticals 355 Riverwalk Parkway, Tonawanda, NY 14150.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0296-2024·2023-10-25

    Kraft Singles American Cheese Recalled for Plastic Film Fragment Risk

    Heinz is recalling Kraft Singles American Cheese because thin plastic film fragments may remain on cheese slices after unwrapping. Affected product was distributed nationwide and in Puerto Rico.

    Product
    Kraft Singles American Pasteurized Prepared Cheese product, 24 individually wrapped slices in flexible film per pack, net wt. per pack 16oz, keep refrigerated. Single pack is sold at retail. Case UPC 0 00 2100007180 7; Single Pack UPC 0 2100061526 1: Each case contains 27…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V715000·2023-10-25

    Porsche 911 GT3 air bag control unit may deploy unnecessarily in crash

    Porsche is recalling certain 2021-2024 911 models equipped with optional full bucket seats due to a potential air bag control defect. Unnecessary air bag deployment during a crash could increase injury risk.

    Product
    PORSCHE — PORSCHE 911 GT3, 911 TURBO, 911 TURBO S, 911 GT3 RS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0044-2024·2023-10-25

    Sun Pharmaceutical Bupropion Extended-Release Tablets Recalled for Failed Dissolution

    Sun Pharmaceutical is recalling Bupropion Hydrochloride Extended-Release Tablets (150 mg), lot HAD0360A, due to failed dissolution specifications. The 144 bottles were distributed nationwide and may not dissolve at the intended rate.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0045-2024·2023-10-25

    Over-the-counter drugs from Family Dollar recalled for improper storage

    Dollar Tree Distribution recalled approximately 4.3 million over-the-counter drug products sold by Family Dollar stores nationwide after discovering they were stored outside of labeled temperature requirements.

    Product
    Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail stores.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0118-2024·2023-10-25

    Medline ReNewal Ligasure Maryland Jaw Sealer devices recalled for incomplete packaging seals

    Medline is recalling 58 units of ReNewal Ligasure Maryland Jaw Sealer electrosurgical instruments due to incomplete seals on packaging trays that may allow contamination during reprocessing.

    Product
    MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider Nano-Coated Complatible with FT10 Generator, REF LF1944CR. electrosurgical instrument
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0117-2024·2023-10-25

    Electrosurgical Devices Recalled for Incomplete Packaging Tray Seal

    Medline is recalling 11 reprocessed Covidien LigaSure and Ethicon Harmonic electrosurgical devices due to incomplete seals on their packaging trays.

    Product
    MEDLINE ReNewal Ligasure Blunt Tip Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF1844CR. electrosurgical instrument
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0043-2024·2023-10-25

    Ophthalmic Solution Recalled Due to Subpotent Ketorolac Levels

    MYDRIATIC-4 ophthalmic solution is being recalled because ketorolac levels fell below the required 90-110% specification. The product was distributed to physician offices nationwide.

    Product
    MYDRIATIC-4: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic Solution Drops 1% - 0.5% - 2.5% - 0.5%, 5mL bottle, Imprimis, NJOF, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852 (844)-446-6979, NDC:71384-632-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0121-2024·2023-10-25

    SenSight Connector Plug Recalled for Use By Date Label Discrepancy

    Medtronic Neuromodulation is recalling 65 units of the SenSight Connector Plug, Model B31061, due to a discrepancy in the Use By Date printed on the device label. The company is requesting return of affected units.

    Product
    SenSight Connector Plug, Model Number B31061.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0119-2024·2023-10-25

    MEDLINE Electrosurgical Instruments Recalled for Incomplete Packaging Seals

    MEDLINE INDUSTRIES is recalling ReNewal Ligasure Sealer/Divider electrosurgical instruments due to incomplete seals on packaging trays. The recall affects 268 units distributed in the United States.

    Product
    MEDLINE ReNewal Ligasure Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF4418CR. electrosurgical instrument
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·23V713000·2023-10-24

    Mack Recalls 2024 LR Trucks Due to Loose Steering Fasteners

    Mack Trucks is recalling 2024 LR vehicles because loose steering fasteners may cause loss of control. Owners should not drive until repaired.

    Product
    MACK — MACK LR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·053-2023·2023-10-23

    Capitology LLC Recalls Ineligible Pork Chicharrones Imported from Honduras

    Capitology LLC is recalling 4,679 pounds of pork chicharrones imported from Honduras because the country is ineligible to export pork to the U.S.

    Product
    Capitology, LLC Recalls Ineligible Pork Chicharrones Products Imported from Honduras
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·23V712000·2023-10-23

    Midwest Automotive Designs Recalls 2017-2022 Motorhomes Due to Wheel Defect

    Midwest Automotive Designs is recalling 2017-2022 motorhomes because alloy wheels may crack and fail, increasing crash risk.

    Product
    MIDWEST AUTOMOTIVE DESIGN — MIDWEST AUTOMOTIVE DESIGN ULTIMATE PRESIDENTIAL, LUXE CRUISER, ULTIMATE CLUB J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V706000·2023-10-20

    Coachmen Concord Motorhomes Recalled for Driveline Angle Defect

    Forest River is recalling 2023-2024 Coachmen Concord motorhomes because an incorrect driveline angle may cause rear wheel lockup and increase crash risk.

    Product
    COACHMEN — COACHMEN CONCORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·052-2023·2023-10-20

    Del Valle Recalls Raw Pork Chorizo Produced Without Federal Inspection

    Del Valle Import and Export LLC is recalling raw pork chorizo produced without federal inspection and bearing a false mark of inspection.

    Product
    Del Valle Import and Export LLC Recalls Pork Chorizo Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V711000·2023-10-20

    New Flyer Transit Buses Recalled for Incorrect Weight Rating Labels

    New Flyer is recalling 2021-2023 transit buses because incorrect weight rating labels may allow vehicles to be overloaded, increasing crash risk.

    Product
    NEW FLYER — NEW FLYER XE40, XD35, XDE35, XD60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V710000·2023-10-20

    2024-2025 Lion School Buses Recalled for Brake System Installation Defect

    Lion Electric is recalling certain 2024-2025 LionC school buses due to incorrect installation of anti-lock brake system pneumatic valve connections and rear wheel speed sensors, which can cause wheel lockup or loss of vehicle control.

    Product
    LION — LION LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V707000·2023-10-20

    BMW Recalls 157,796 Vehicles for Potential Engine Stall Risk

    BMW is recalling 157,796 vehicles from 2010-2012 because aluminum bolts securing the VANOS unit may loosen or break, potentially causing an engine stall and increasing crash risk.

    Product
    BMW — BMW X5, Z4, 3 SERIES, 1 SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24011·2023-10-19

    Fortress Safe Biometric Gun Safes: Unauthorized Access and Risk of Death

    Xpedition LLC is recalling approximately 61,000 biometric gun safes because the biometric locks can be opened by unauthorized users, posing serious injury and death risks. One death has been reported in a recent lawsuit.

    Product
    Biometric Gun Safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·051-2023·2023-10-19

    USDA Recalls Ineligible Imported Pork Chicharrones from East Coast Food Distributors

    USDA FSIS is recalling approximately 7,767 pounds of pork chicharrones imported from Colombia because the country is ineligible to export meat to the U.S.

    Product
    East Coast Food Distributors, Inc. Recalls Ineligible Pork Chicharrones Products Imported from Colombia
    Category
    Food
    Distribution
    Distributed nationwide