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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15476–15500 of 36693

  • CriticalFDA (Drugs)·D-0360-2019·2018-12-26

    Lubrisine eye drops recalled for undeclared colloidal silver and sterility issues

    Results RNA, LLC is recalling Lubrisine eye drops nationwide due to lack of sterility assurance and the presence of undeclared colloidal silver.

    Product
    Lubrisine eye drops (polyethylene glycol 400 0.4% and Propylene glycol 0.3%), 30 ML bottle, Manufactured and Distributed by: Results RNA, LLC, 1272 S 1380 W., Orem, UT 84058, UPC 7 9238230723 4
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0748-2019·2018-12-26

    Bakkavor Baked Macaroni and Cheese Recalled for Undeclared Allergens

    Bakkavor Foods USA Inc. is recalling Baked Macaroni and Cheese because it contains lobster, shrimp, and soy that are not listed on the label.

    Product
    Baked Macaroni and Cheese, NET WT 12 OZ (340g), CONTAINS: WHEAT, MILK, EGG, Produced By BAKKAVOR USA, 2700 Westinghouse Blvd. Charlotte, NC 28273, Phone: 704-522-1977, UPC 7 61088 80502 3
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0776-2019·2018-12-26

    Lipari Foods Recalls Inspired Organic Almond Butter Due to Listeria

    Lipari Foods is recalling Inspired Organic Almond Butter because product testing found Listeria monocytogenes. Consumers should stop using the product.

    Product
    Inspired Organic Almond Butter 16oz. plastic jar, 6 per case UPC #: 863669742540 refrigerate after opening
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·F-0729-2019·2018-12-26

    Galil Seasoned Tahini Recalled Due to Salmonella Contamination Risk

    Achdut is recalling Galil Seasoned Tahini because it may be contaminated with Salmonella. The product was distributed in New York, California, Pennsylvania, and Israel.

    Product
    Seasoned Tahini sold under the following brand name: Galil Seasoned Tahini, 500g, UPC: 814968020020
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0777-2019·2018-12-26

    Inspired Organic Tahini Butter Recalled for Listeria monocytogenes Contamination

    Lipari Foods is recalling Inspired Organic Tahini Butter because product testing confirmed the presence of Listeria monocytogenes.

    Product
    Inspired Organic Tahini Butter 16oz. plastic jar, 6 per case UPC #: 863669742564 refrigerate after opening
    Category
    Food
    Distribution
    15 states
  • CriticalFDA (Food)·F-0726-2019·2018-12-26

    Marich Recalls Milk Chocolate Maltballs Due to Undeclared Macadamia Nuts

    Marich Confectionery is recalling 15 lb cases of Milk Chocolate Maltballs because a customer found undeclared macadamia nuts in the shipment.

    Product
    Milk Chocolate Maltballs: NET Wt. 15 lbs. Item number 992 Case UPC 00797817-00992-9 Allergy Information: This product contains Wheat, milk and soy and may contain peanuts and tree nuts.
    Category
    Food
    Distribution
    23 states
  • CriticalFDA (Food)·F-0728-2019·2018-12-26

    Achdut Recalls Raw Tahini Products Due to Salmonella Contamination Risk

    Achdut is recalling specific lots of raw tahini because the product may be contaminated with Salmonella. The recall affects units distributed to New York, California, Pennsylvania, and Israel.

    Product
    Raw Tahini sold under the following brand names: Baron's raw Tahini, 454g, UPC: 816412010083; Soom raw Tahini 220kg (no barcode on product); Soom raw Tahini 18kg, UPC: 718088347329; Soom raw Tahini, 454g, UPC: 718088347411
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0770-2019·2018-12-26

    Luckyberry Recalls Unpasteurized Cold-Pressed Spicy Ginger Juice

    Luckyberry is recalling unpasteurized Spicy Ginger cold-pressed juice sold in Lawrence, KS, due to a violation of FDA juice safety regulations.

    Product
    Luckyberry Cold-Pressed Juice, Spicy Ginger, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0769-2019·2018-12-26

    Luckyberry Recalls Unpasteurized Cold-Pressed Juice for Regulatory Violation

    Luckyberry is recalling unpasteurized cold-pressed juice sold in Lawrence, Kansas, due to violations of FDA juice safety regulations.

    Product
    Luckyberry Cold-Pressed Juice, Merc Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0497-2019·2018-12-26

    COVIDIEN Recalls Puritan Bennett 980 Ventilators Due to Software Update Issues

    COVIDIEN LLC is recalling 9,593 Puritan Bennett 980 ventilators worldwide due to a software update affecting external USB drive performance and GUI functionality.

    Product
    Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980 Pediatric Adult Ventilator Puritan Bennett" 980 Neonatal Ventilator Puritan Bennett" 980 Universal Ventilator Product Usage: The Puritan Bennett 980 Series Ventilator is designed for use on patient…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0766-2019·2018-12-26

    Luckyberry Cold-Pressed Juice Recalled for Unpasteurized Juice Violations

    Luckyberry is recalling cold-pressed juice products sold in Lawrence, KS, because they were manufactured and distributed in violation of FDA regulations requiring pasteurization.

    Product
    Luckyberry Cold-Pressed Juice, NoCoast, Kale, Cucumber, Green Apple, Celery, Lemon, Ginger, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0354-2019·2018-12-26

    Enovachem Recalls Dyural-80 Injection Kits Due to Incorrect Latex Labeling

    Enovachem is recalling Dyural-80 Injection Kits because the product insert incorrectly stated that the stoppers do not contain latex, when they actually contain natural rubber latex.

    Product
    Dyural-80 Injection Kit, 1 Dose, Single Use Only, Rx only, Distributed by Enovachem Pharmaceuticals, Torrance, CA 90501, NDC 76420-0755-01
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0337-2019·2018-12-26

    Tris Pharma Recalls Infants' Ibuprofen Due to Higher Concentration

    Tris Pharma is recalling specific lots of Infants' Ibuprofen because they may contain a higher concentration of the active ingredient.

    Product
    Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye Free, Non-staining Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 39338 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0771-2019·2018-12-26

    Luckyberry Recalls Unpasteurized Cold-Pressed Juice for Regulatory Violations

    Luckyberry is recalling unpasteurized cold-pressed juice products distributed in Lawrence, Kansas, due to violations of FDA juice safety regulations.

    Product
    Luckyberry Cold-Pressed Juice, Seasonal Blend, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0353-2019·2018-12-26

    Dyural-40 Injection Kit Recalled for Incorrect Latex Labeling

    Asclemed USA Inc. is recalling Dyural-40 Injection Kits because the product insert incorrectly states that the stoppers do not contain latex, when they actually do.

    Product
    Dyural-40 Injection Kit, 1 Dose, Single Use Only, Rx only, Distributed by Enovachem Pharmaceuticals, Torrance, CA 90501, NDC 76420-0750-01
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0626-2019·2018-12-26

    FDA Recalls Covidien Emprint Percutaneous Antenna Due to Tip Disengagement

    FDA is recalling specific lots of the Covidien Emprint Short Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft during use, potentially remaining in the patient.

    Product
    Covidien Emprint Short Percutaneous Antenna with Thermosphere Technology, Material CA15L2 intended for use in percutaneous, laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of nonresectable liver tumors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0336-2019·2018-12-26

    Tris Pharma Recalls Superpotent Infants' Ibuprofen Suspension

    Tris Pharma is recalling 19,488 bottles of Infants' Ibuprofen due to potential higher-than-labeled ibuprofen concentrations.

    Product
    Infants' Ibuprofen, Concentrated Ibuprofen Oral Suspension, USP, (NSAID), 50 mg per 1.25 mL, Dye-Free Non-Staining Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by Family Dollar Services, Inc., 10301 Monroe Road, Matthews, NC 28105, NDC 55319-250-23, UPC 0 32251 03374 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0335-2019·2018-12-26

    Tris Pharma Recalls Infants' Ibuprofen Due to Higher Concentration

    Tris Pharma is recalling specific lots of infants' ibuprofen oral suspension because they may contain a higher concentration of the active ingredient.

    Product
    infants* IBUPROFEN, Concentrated Ibuprofen Oral Suspension, USP (NSAID), 50 mg per 1.25 mL, Dye-Free Berry Flavor, 0.5 FL OZ (15 mL) bottle, Distributed by Wal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-125-23, UPC 0 78742 02016 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0772-2019·2018-12-26

    Luckyberry Cold-Pressed Beetnik Juice Recalled for Unpasteurized Status

    Luckyberry is recalling cold-pressed Beetnik juice sold in Lawrence, KS, because the product was manufactured and distributed in violation of FDA regulations requiring pasteurization.

    Product
    Luckyberry Cold-Pressed Juice, Beetnik, Orange, Red Beet, Kale, Cucumber, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0615-2019·2018-12-26

    Abbott i-STAT CG8+ Cartridges Recalled for Inaccurate Potassium Results

    Abbott Point Of Care Inc. is recalling i-STAT CG8+ Cartridges because they may generate inaccurate potassium results, potentially leading to incorrect clinical decisions.

    Product
    Abbott i-STAT CG8+ Cartridges intended for use in the in vitro quantification of potassium in arterial, venous, or capillary whole blood. List Number/UDI# : 03P88-25 ,(01)10054749000163(17)181028(10)L18059
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0333-2019·2018-12-26

    Pharmedium Recalls Sub-Potent Fentanyl and Ropivacaine Injection Syringes

    Pharmedium Services, LLC is voluntarily recalling 295 syringes of a fentanyl and ropivacaine injection that were found to be sub-potent.

    Product
    Fentanyl Citrate 2 mcg per mL (100 mcg per 50 mL) and Ropivacaine HCl 0.1% in Sodium Chloride 0.9%, Injection, 50 mL total volume in a 60 mL BD Syringe, Rx Only, PharMEDium Services, LLC. 913 N. Davis Ave. Cleveland, MS 38732 NDC 61553-644-75.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0627-2019·2018-12-26

    FDA Recalls Covidien Emprint Percutaneous Ablation Antenna Due to Tip Disengagement

    FDA is recalling the Covidien Emprint Standard Percutaneous Antenna because the ceramic trocar tip may disengage from the needle shaft, potentially remaining in the patient.

    Product
    Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology, CA20L2 intended for use in percutaneous, laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of nonresectable liver tumors.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0778-2019·2018-12-26

    Lipari Foods Recalls Inspired Organic Peanut Butter for Listeria

    Lipari Foods Operating Company, LLC is recalling Inspired Organic Peanut Butter after product testing returned positive results for Listeria monocytogenes.

    Product
    Inspired Organic Peanut Butter 16oz. plastic jar, 6 per case UPC #: 863669742588 refrigerate after opening
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Drugs)·D-0343-2019·2018-12-26

    Pharm D Solutions Recalls Human Chorionic Gonadotropin Vials Due to Sterility Concerns

    Pharm D Solutions is recalling 85 vials of Human Chorionic Gonadotropin 3000 IU due to inadequate processes to assure sterility.

    Product
    Human Chorionic Gonadotropin 3000 IU, Rx only, Pharm D. Solutions 1304 South Loop West, Houston, TX 77054 1-844-263-6843 --- NDC: 69699-1738-10
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0774-2019·2018-12-26

    Luckyberry Recalls Unpasteurized Cold-Pressed Juice for Regulatory Violation

    Luckyberry is recalling unpasteurized Mai Tai and Orange Pineapple cold-pressed juices sold in Lawrence, Kansas, due to violations of FDA juice safety regulations.

    Product
    Luckyberry Cold-Pressed Juice, Mai Tai, Orange Pineapple, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS
    Category
    Food
    Distribution
    0 states