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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34476–34500 of 39756

  • SevereFDA (Drugs)·D-613-2013·2013-07-03

    Hospira Recalls Sodium Chloride Injection Due to Sterility Concerns

    Hospira is voluntarily recalling 0.45% Sodium Chloride Injection due to possible leaking bags that may compromise sterility.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1575-2013·2013-07-03

    Medtronic Recalls INDURA 1P Intrathecal Catheters Due to Occlusion Risk

    Medtronic is recalling INDURA 1P Intrathecal Catheters because the previous connector design has a greater potential for misalignment and occlusion.

    Product
    Medtronic INDURA 1P Intrathecal Catheter, model 8709SC. Contents: 81.4-cm catheter with length markers and guide wire, 15 T-gauge introducer needle, Sutureless pump connector with attached 7.6-cm catheter and Connector pin, Transparent Strain-relief sleeves, and anchors.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1580-2013·2013-07-03

    Medtronic SynchroMed EL Pumps Recalled for Electrical Shorting Risk

    Medtronic is recalling SynchroMed EL pumps due to potential internal electrical shorting that may cause therapy loss.

    Product
    Medtronic SynchroMed EL Programmable pumps, Models 8626, 8626L, 8627, 8627L, (The SynchroMed EL Pumps are supplied in 10 ml or 18 ml reservoir size.) Sterilized using ethylene oxide. The pump is part of an infusion system that stores and delivers a prescribed drug to a specific…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1574-2013·2013-07-03

    Taylor Farms Recalls Black Forest Ham and Cheese Pretzel Rolls

    Taylor Farms is recalling Black Forest Ham and Cheese Pretzel Rolls due to potential undeclared tree nut allergens.

    Product
    Wawa Black Forest Ham and Cheese on a Pretzel Roll with swiss cheese and country dijon honey mustard. Net Wt. 8.7 oz (247g). Distributed by Wawa, Inc., Wawa, PA 19063.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1576-2013·2013-07-03

    See's Candies Recalls Dark and Milk Chocolate Covered Raisins for Allergen Risk

    See's Candies is recalling 4,700 pounds of dark and milk chocolate covered raisins due to potential nut and egg residue.

    Product
    See's Dark Raisins: Ingredients: Raisins, Sugar,chocolate, cocoa butter, butter (milk), vanilla, soy lecithin, Dextrin, Confectionery glaze. May contain traces of eggs, tree nuts and peanuts. Sold in Net Wt. 8 oz (227 g) clear plastic packages or purchased by customer…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-611-2013·2013-07-03

    Hospira Recalls 0.9% Sodium Chloride Injection Due to Sterility Concerns

    Hospira is voluntarily recalling 0.9% Sodium Chloride Injection in flexible containers due to possible leaking bags that may compromise sterility.

    Product
    0.9% Sodium Chloride Injection, USP, Polyolefin Flexible Container, a) 500 mL (NDC 0409-7983-30), b) 1000 mL (NDC 0409-7983-48), c) 250 mL (NDC 0409-7983-02), d) 150 mL (NDC 0409-7983-61), Rx Only, by Hospira, Inc., Lake Forest, IL 60045
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-616-2013·2013-07-03

    Hospira Recalls 20% Dextrose Injection Due to Possible Leaking Bags

    Hospira is voluntarily recalling 20% Dextrose Injection, USP, due to possible leaking bags that may compromise sterility.

    Product
    20% Dextrose Injection, USP, a) 500 mL in 1000 mL Partial-Fill Container (NDC 0409-7935-19), b) 500 mL VisIV Container (NDC 0409-7953-30), c) 1000 mL VisIV Container, (NDC 0409-7953-48), Rx Only, Hospira, Inc., Lake Forest, IL 60045
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-617-2013·2013-07-03

    Hospira Recalls 0.9% Sodium Chloride Irrigation Due to Sterility Concerns

    Hospira is voluntarily recalling 0.9% Sodium Chloride Irrigation bags due to possible leaking that compromises sterility.

    Product
    0.9% Sodium Chloride Irrigation, USP, 3000 mL, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7972-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V293000·2013-07-03

    Dutchmen Recalls 2013-2014 Travel Trailers Due to Propane Hose Fire Risk

    Dutchmen is recalling 2013-2014 Aspen, Coleman, and Dutchmen travel trailers because heat from the range burner may melt the propane supply hose, increasing the risk of a fire.

    Product
    ASPEN TRAIL — ASPEN TRAIL, COLEMAN, DUTCHMEN TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1576-2013·2013-07-03

    Medtronic Recalls Sutureless Connector Intrathecal Catheters Due to Occlusion Risk

    Medtronic is recalling 115,722 Sutureless Connector Intrathecal Catheters worldwide because the previous design has a greater potential for misalignment and occlusion.

    Product
    Medtronic Intrathecal Catheter, model 8731SC. Contents: 38.1-cm spinal segment with length markings and guide wire, 66-cm pump segment, 15 T-gauge introducer needle, Transparent Strain-relief sleeves, Opaque Strain-relief sleeves, and V-wing anchors. Contents of inner package…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1559-2013·2013-07-03

    BIMBO Bakeries Recalls Great Value Hamburger Buns Due to Metal Fragments

    BIMBO Bakeries USA is recalling Great Value 8 Jumbo Hamburger Buns due to possible metal fragments from a faulty manufacturing part.

    Product
    Great Value 8 Jumbo Hamburger Buns Distributed By: Wal-Mart Stores, inc., Bentonville, AR 72716
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1568-2013·2013-07-03

    BIMBO Bakeries Recalls Whole Wheat Hamburger Buns Due to Metal Fragments

    BIMBO Bakeries USA is recalling 12-count packs of Foodservice 100% Whole Wheat Hamburger Buns due to the possible presence of metal fragments caused by a faulty manufacturing part.

    Product
    Foodservice 100% Whole Wheat Hamburger Buns - 12 Ct Earthgrains Baking companies, Inc. Horsham, PA 19044
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1571-2013·2013-07-03

    Medtronic SynchroMed EL Pumps Recalled for Unintended Drug Delivery

    Medtronic is recalling SynchroMed EL implantable pumps due to a risk of unintended drug delivery during the priming bolus function, which may cause overdose or underdose.

    Product
    Medtronic SynchroMed EL Programmable pumps, Models 8626, 8626L, 8627, 8627L, (The SynchroMed EL Pumps are supplied in 10 ml or 18 ml reservoir size.) Sterilized using ethylene oxide. Product Usage: The pump is part of an infusion system that stores and delivers a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-618-2013·2013-07-03

    Hospira Recalls 1.5% Glycine Irrigation Due to Sterility Concerns

    Hospira is voluntarily recalling 1.5% Glycine Irrigation, USP, 3000 mL, due to possible leaking bags that may compromise sterility.

    Product
    1.5% Glycine Irrigation, USP, 3000 mL, Rx Only, Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7974-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1560-2013·2013-07-03

    BIMBO Bakeries USA Recalls Kerns Beef Buns Due to Metal Fragments

    BIMBO Bakeries USA is recalling 812 cases of Kerns Beef Buns due to possible metal fragments from a faulty manufacturing part.

    Product
    Kerns Beef Buns - 12 count Distributed By: K-VA-T Food Stores, Inc., Arbingdon, VA 24210
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·13V292000·2013-07-03

    Toyota Recalls 2012 Yaris Vehicles for Power Steering Defect

    Toyota is recalling 2012 Yaris vehicles because a relay in the power steering system could short-circuit, disabling steering assistance and increasing crash risk.

    Product
    TOYOTA — TOYOTA YARIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1579-2013·2013-07-03

    Medtronic SynchroMed II Pumps Recalled for Electrical Shorting Risk

    Medtronic is recalling SynchroMed II pumps due to potential electrical shorting that may cause therapy loss or reduction.

    Product
    Medtronic SynchroMed II, Model 8637, (The SynchroMed II Pump is supplied in 20 ml or 40 ml reservoir size.) Sterilized using ethylene oxide. The pump is part of an infusion system that stores and delivers a prescribed drug to a specific site. The implantable components of the…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1569-2013·2013-07-03

    BIMBO Bakeries Recalls Earthgrains Hamburger Buns Due to Metal Fragments

    BIMBO Bakeries USA is recalling Earthgrains Food Service Hamburger Buns Wheat with Oat due to possible metal fragments from a faulty manufacturing part.

    Product
    Food Service Hamburger Buns Wheat with Oat 12 CT Earthgrains Baking companies, Inc. Horsham, PA 19044
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1575-2013·2013-07-03

    See's Candies Recalls Milk Raisins for Potential Nut and Egg Residue

    See's Candies is recalling 5,814 pounds of Milk Raisins because they may contain undeclared nut or egg residues. The product was sold in 240 stores and 10 licensees nationwide.

    Product
    See's Milk Raisins: Ingredients: Raisins, Sugar, Cocoa butter, milk chocolate, soy lecithin, Vanillin, Dextrin, Confectionery glaze.May contain traces of eggs, tree nuts and peanuts Sold in Net Wt. 8 oz (227 g) clear plastic packages or purchased by customer at counter in…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1574-2013·2013-07-03

    Medtronic Recalls Intrathecal Catheter Pump Segment Revision Kits

    Medtronic is recalling unused Model 8596SC Pump Segment Revision Kits due to a design flaw that increases the risk of catheter occlusion.

    Product
    Medtronic Intrathecal Catheter Pump Segment Revision Kit, model 8596SC. Contents: 60-cm pump segment with attached sutureless pump connector, Spinal Segment Strain-relief sleeves, Pump segment strain-relief sleeves, Connector pin. Contents of inner package are STERILE. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-615-2013·2013-07-03

    Hospira Recalls 5% Dextrose and 0.45% Sodium Chloride Injection Due to Sterility Concerns

    Hospira Inc. is voluntarily recalling 74,256 units of 5% Dextrose and 0.45% Sodium Chloride Injection due to possible leaking bags that may compromise sterility.

    Product
    5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-48
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1558-2013·2013-07-03

    BIMBO Bakeries Recalls Colonial Seeded Buns Due to Metal Fragments

    BIMBO Bakeries USA is recalling Colonial 12 Seeded Enriched Buns due to possible metal fragments from a faulty manufacturing part.

    Product
    Colonial 12 Seeded Enriched Buns Sara Lee, Downers, Grove, IL 60515
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-612-2013·2013-07-03

    Hospira Recalls 70% Dextrose Injection Due to Possible Leaking Bags

    Hospira is voluntarily recalling 14,706 units of 70% Dextrose Injection USP due to possible leaking bags that may compromise sterility.

    Product
    70% Dextrose Injection USP, 2000 mL, Rx Only, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7120-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1572-2013·2013-07-03

    Bimbo Bakeries Recalls Hamburger Buns Due to Possible Metal Fragments

    Bimbo Bakeries USA is recalling food service hamburger buns due to the possible presence of metal fragments caused by a faulty manufacturing part.

    Product
    Hamburger Buns Bimbo Bakeries USA 255 Business Center Dr. Horsham, PA 19044 Food Service Hamburger Buns, Seeded and Unseeded, all counts:
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1586-2013·2013-07-03

    Medrad Recalls DC Power Cables for Veris MR Vital Signs Monitor

    Medrad Inc is recalling 1,066 DC power cables for the Veris MR Vital Signs Monitor due to a design issue that could cause shorting and heating.

    Product
    DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor, Physiological, Patient
    Category
    Medical Device
    Distribution
    Distributed nationwide