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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24376–24400 of 90113

  • HighFDA (Drugs)·D-1245-2022·2022-07-27

    Nephron Amino Acid Injection Bags Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling 163 bags of Amino Acid Injection due to lack of assurance of sterility. Patients using this intravenous medication should contact their healthcare provider immediately.

    Product
    Amino Acid Injection 50 g/1000 mL (50 mg/mL) bags, Rx Only, Nephron 503B outsourcing facility, 4500 12th Extension, West Columbia, SC 29172, NDC: 69374-988-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1259-2022·2022-07-27

    Ketamine HCl Injection Recalled Due to Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling Ketamine HCl Injection due to lack of sterility assurance. The recall affects 91,445 pre-filled syringes distributed nationwide.

    Product
    Ketamine HCl Injection, USP, 50 mg/5 mL (10 mg/mL*) syringes, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-982-55
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1478-2022·2022-07-27

    Honey caramels recalled for undeclared tree nut allergen

    Queen Bee Gardens is recalling Honey Caramels The Mint due to undeclared tree nuts. The product may contain pecans, almonds, coconut, macadamia nuts, or walnuts.

    Product
    Honey Caramels The Mint. Net wt. 5.87 oz. PLU Code: 788394 12760 1. Ingredients: Honey, butter (pasteurized cream & salt), cream, nonfat dry milk, whey, 100% pure essential peppermint oil, lecithin, algin & agar.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1266-2022·2022-07-27

    Morphine Sulfate Injection Recalled Due to Lack of Sterility Assurance

    Nephron Sterile Compounding Center LLC is recalling Morphine Sulfate Injection due to lack of assurance of sterility. The recall affects 8,985 syringes distributed nationwide.

    Product
    Morphine Sulfate Injection, USP, 30 mg/30 mL (1 mg/mL) syringe, packaged in 5 x 30 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-979-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1254-2022·2022-07-27

    Glycopyrrolate Syringes Recalled Due to Sterility Assurance Failure

    Nephron Sterile Compounding Center is recalling 3450 glycopyrrolate injection syringes (NDC 69374-903-30, Lot GL2004A) nationwide due to lack of assurance of sterility.

    Product
    Glycopyrrolate Injection, USP, 0.6 mg/3 mL (0.2 mg/mL) syringes, packaged in 5 x 3 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-903-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1410-2022·2022-07-27

    Modulift VBR Surgical Screwdriver Fails Due to Tip Deformation

    Aesculap is recalling the Modulift VBR 4MM set screwdriver due to tip deformation during surgical engagement with implants. The device is distributed in CA, FL, GA, IL, OH, and MI.

    Product
    MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Food)·F-1439-2022·2022-07-27

    Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Lecithin

    Chuckanut Bay Foods recalls cheesecake bites for undeclared soy lecithin in the chocolate compound. The label incorrectly states sunflower lecithin, creating an allergic reaction risk for consumers with soy allergies.

    Product
    Item 34021-12, Chuckanut Bay Cheesecake Bites Berry. Perishable - Keep Refrigerated. There are 8 pieces per pack and 12 packs per case. Net Wt. 6.4 oz. UPC 6 03812 34021 2. Item 35009-12, Chocolate Covered Berry Cheesecake Bites. Edible brand. Distributed by Wish Foods…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1388-2022·2022-07-27

    Hobbs Medical Polypectomy Snare May Fail to Close Properly

    Hobbs Medical Polypectomy Snares (Catalog No. 7202) may accordion at the proximal end, preventing full closure and potentially causing injury. Specific lots distributed to medical facilities in NC, TX, WA, and Canada are affected.

    Product
    Hobbs Medical Polypectomy Snare, Catalog No. 7202
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-1447-2022·2022-07-27

    Chuckanut Bay Cheesecake Bites recalled for undeclared soy allergen

    Chuckanut Bay Foods is recalling Dipped Cheesecake Bites (Pumpkin) because the product contains undeclared soy lecithin. The label incorrectly lists sunflower lecithin, creating a health risk for consumers with soy allergies.

    Product
    Item 39408-12, Chuckanut Bay DIPPED CHEESECAKE BITES Pumpkin. Perishable - Keep Refrigerated. There are 4 pieces per pack and 12 packs per case. Net wt. 3.2 oz per package. UPC 6 03812 39408 6. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, PUMPKIN, CANE…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1485-2022·2022-07-27

    Honeymoons Milk Chocolate Cashew recalled for undeclared tree nuts

    Queen Bee Gardens is recalling Honeymoons Milk Chocolate Cashew candy due to undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. Consumers with tree nut allergies face potential serious health risks.

    Product
    Honeymoons Milk Chocolate Cashew. PLU Code: 788394 14828 6
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1415-2022·2022-07-27

    Medical Bed Mattress Microclimate Failure Increases Pressure Ulcer Risk

    Affected Hill-Rom Centrella Pro+ hospital mattresses can fail to properly manage heat and moisture removal, increasing the risk of pressure ulcer development in patients.

    Product
    Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1255-2022·2022-07-27

    HYDROmorphone Injection Recalled Due to Lack of Sterility Assurance

    Nephron Sterile Compounding Center recalled 22,805 pre-filled syringes of HYDROmorphone HCl Injection due to lack of sterility assurance. Six lot numbers were distributed nationwide.

    Product
    HYDROmorphone HCl Injection, USP, 10 mg/50 mL (0.2 mg/mL) syringes, 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th Street Extension, West Columbia SC 29172, NDC: 69374-529-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1457-2022·2022-07-27

    Dark chocolate truffles recalled for undeclared tree nut allergens

    Queen Bee Gardens is recalling Dark Mint Classic Truffles for undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Products were distributed to retail locations in CO, NM, WY and nationwide online.

    Product
    Dark Mint Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11035 1. Ingredients: Dark chocolate, honey, butter (pasteurized cream & salt), cream, dry milk, whey, agar, algin, lecithin & peppermint oil. Decoration: "Ivory" chocolate & artificial color.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1471-2022·2022-07-27

    Honey Caramels Almond Coconut Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Almond Coconut due to potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Consumers allergic to tree nuts should not consume this product.

    Product
    Honey Caramels Almond Coconut. Product available in 5.87 oz. bag, 1 lb. bag, 3 lb. bag, 6 lb. bag. PLU Code for 5.87 oz bag: 788394 12004 6. Ingredients: Honey, butter (pasteurized cream & salt), cream, almonds, coconut, nonfat dry milk, whey, natural flavors, lecithin…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1452-2022·2022-07-27

    SurgiCount+ System software error bypasses sponge tracking alerts

    A software error in SurgiCount+ System Application may allow duplicate surgical sponges to be counted without the required documentation prompt. This could allow surgical cases to close without proper verification that all sponges were accounted for.

    Product
    SurgiCount+ System Application, Software Version 2.0.17, Catalog Number 0694-002-090. Used for counting, displaying, recording and locating the number of RFID-tagged absorbent articles used during surgical procedures.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1408-2022·2022-07-27

    Nonsterile convenience kit recall due to sterile component mislabeling

    ROi CPS LLC is recalling 40 nonsterile convenience kits (Lot #92605) because sterile components were incorrectly packaged as nonsterile. The affected kits were distributed in Missouri.

    Product
    Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1424-2022·2022-07-27

    Randox Cholesterol In Vitro Diagnostic Kits Fail Stated Performance Specifications

    Randox Cholesterol diagnostic kits fail to meet stated performance specifications. Calibration issues cause quality control results to fall outside acceptable ranges, potentially delaying test results.

    Product
    Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1487-2022·2022-07-27

    Chocolate Cashew Candy Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honeymoons Ivory Chocolate Cashew candy because it may contain undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts, which can cause severe allergic reactions.

    Product
    Honeymoons Ivory Chocolate Cashew. PLU Code: 788394 14900 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1461-2022·2022-07-27

    Queen Bee Gardens Huckleberry Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Huckleberry Truffles because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide via internet.

    Product
    Huckleberry Truffle. Net wt. 1.4 oz. PLU Code: 788394 11057 3. Ingredients: Dark chocolate (sugar, chocolate liquor processed with potassium carbonate, cocoa butter, milk fat [butter], HONEY, "Ivory" chocolate (sugar, cocoa butter, whole & non-fat milk solids, sunflower…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1264-2022·2022-07-27

    Lidocaine HCl injection syringes recalled due to sterility assurance failure

    Nephron Sterile Compounding Center has recalled 37,310 syringes of Lidocaine HCl Injection USP 1% nationwide due to lack of assurance of sterility. Affected lots expire between August and October 2022.

    Product
    Lidocaine HCl Injection, USP 1%, 50 mg/5 mL (10 mg/mL) syringe, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-985-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1409-2022·2022-07-27

    Aesculap Aeos Digital Microscope robotic arm malfunction requires system restart

    Aesculap Implant Systems is recalling the UR5 robotic arm component in its Aeos Digital Microscope System due to malfunction that prevents arm movement and requires system restart.

    Product
    Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-1444-2022·2022-07-27

    Cheesecake Bite Products Recalled for Undeclared Soy Allergen Mislabeling

    Chuckanut Bay Foods LLC is recalling cheesecake bite products with labels declaring sunflower lecithin when they actually contain soy lecithin. Soy is a major allergen not properly disclosed to consumers.

    Product
    Item 35001-12, Chocolate Covered CHEESECAKE BITES NY SIGNATURE. Edible brand. Distributed by Wish Foods, LLC. Perishable - Keep Refrigerated. There are 8 pieces per pack and 12 packs per case. Net Wt. 6.4 oz. UPC 8 50014 91804 0. Item 39401-12, Chuckanut Bay DIPPED…
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1464-2022·2022-07-27

    Bee Energy Bar recalled due to undeclared tree nuts

    Queen Bee Gardens is recalling Bee Energy Bars due to undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. Consumers with tree nut allergies should not consume this product.

    Product
    Bee Energy Bar. Net wt. 1.5 oz. PLU Code: 788394 18559 5. Ingredients: Dark chocolate (sugar, chocolate liquor, cocoa butter, milk fat [butter], sunflower lecithin, pure vanilla), honey, almonds, butter (pasteurized cream, salt), coconut, gluten free oats, dried…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1436-2022·2022-07-27

    Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Lecithin

    Chuckanut Bay Foods is recalling Cheesecake Bites that contain undeclared soy lecithin, listed on the label as sunflower lecithin. Consumers with soy allergies may face serious risk.

    Product
    Item 38180-12, Chuckanut Bay Cheesecake Bites New York + Chocolate. Perishable - Keep Refrigerated. There are 8 pieces per plastic clamshell pack and 12 packs per case. Net wt. per pack 6.4 oz. UPC 6 03812 38180 2. The label is read in parts: "***INGREDIENTS: CREAM…
    Category
    Food
    Distribution
    13 states
  • SevereNHTSA·22V539000·2022-07-26

    Spartan Fire Recalls 2020-2021 Metrostar and Gladiator Trucks for Fire Risk

    Spartan Fire is recalling 2020-2021 Metrostar and Gladiator fire trucks because a loose electrical connection may cause the load center to overheat and increase the risk of a fire.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide