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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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

27051–27075 of 39747

  • SevereFDA (Devices)·Z-2110-2015·2015-07-29

    Surgical Set Up Kits Recalled Due to Sterility Compromise in Gloves

    FDA is recalling 33,256 surgical set up kits containing Devon Light Gloves that have splits or holes compromising sterility.

    Product
    Surgical Set Up kit, Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description: 31144895 7614-T4 Single Basin Set Up Kit 31144960 7693-T4 Single Basin Set Up Kit 31144978 7766 Double Basin Set Up Kit 31145215 7896 Double Basin Set Up Kit 31145231 7897…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2197-2015·2015-07-29

    Philips GEMINI TF Ready CT/PET System Software Defect Recall

    Philips is recalling GEMINI TF Ready CT/PET systems due to software defects that may cause incorrect radiation treatment.

    Product
    GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Systems are a family of integrated diagnostic X-ray Computed Tomography (CT) and Positron Emission Tomography (PET) systems suitable for a wide range of diagnostic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·15200·2015-07-29

    Jenn-Air Wall Ovens Recalled for Burn Risk from Roller Rack

    Whirlpool is recalling Jenn-Air wall ovens because the extendable roller rack can unexpectedly disengage, posing a burn risk. Consumers should stop using the rack and contact Whirlpool for a free repair.

    Product
    Jenn-Air Single, Double Wall Ovens and Combination Microwave/Wall Ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2859-2015·2015-07-29

    Golden Plains Recalls Roseli Sundried Tomato Pesto Sauce for Salmonella

    Golden Plains Frozen Foods is recalling Roseli Sundried Tomato Pesto sauce because it tested positive for Salmonella. The product was contained and not distributed to consumers.

    Product
    Roseli Sundried Tomato Pesto sauce. #408744 (Dot Item) , # 627328 (Roseli item),3- 2 lbs tubs (poly) packed in corrugated shipper. Keep Frozen - Thaw under refrigeration.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2175-2015·2015-07-29

    FDA Recalls Fiber Stripper Tools Due to Sterilization Validation Issues

    American Medical Systems is recalling Fiber Stripper tools because cleaning and sterilization validation data do not meet FDA guidance for reusable products.

    Product
    Tool, Stripper W/BLD, 12S, Autoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureFlex Fiber. The Fiber Stripper does not come in to direct contact with the patient. It is available in several sizes…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2865-2015·2015-07-29

    GloryBee Recalls Turkish Organic Diced Apricots Containing Rocks and Metal

    GloryBee Inc is recalling 107 boxes of Turkish Organic Diced Apricots with Rice Flour due to the presence of rocks and metal.

    Product
    Turkish Organic Diced Apricots with Rice Flour (5-7 mm), FOODIMPEX brand, Item# 17496, product is packged in a white cardboard box. Net wt. 28 lbs.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-2857-2015·2015-07-29

    Marine Harvest Recalls Kirkland Signature Fresh Farmed Atlantic Salmon Fillets

    Marine Harvest is recalling Kirkland Signature fresh farmed Atlantic salmon fillets due to potential Listeria monocytogenes contamination.

    Product
    Kirkland Signature Fresh Farmed Atlantic Salmon Fillet Product of Chile Processed in USA approx 2lbs. Packaged in a styrofoam tray and wrapped in plastic.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2138-2015·2015-07-29

    DePuy ATTUNE Knee Trial Instrument Recall for Balseal Disassociation Risk

    DePuy Orthopaedics is recalling ATTUNE Knee Tibial Articulation Surface Instruments because a small wire spring coil may detach and be left in patients during surgery.

    Product
    ATTUNE FB CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a total knee replacement. A Balseal is attached to each of the two post features on the Articulation…
    Category
    Medical Device
    Distribution
    51 states
  • SevereFDA (Devices)·Z-2136-2015·2015-07-29

    Volcano Intravascular Ultrasound Systems Recalled for Inaccurate FFR/iFR Values

    Volcano Corporation is recalling s5/s5i/CORE Intravascular Ultrasound Systems due to a software issue that may calculate inaccurate FFR/iFR values.

    Product
    Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3 and 3.4 (with and without iFR Scout Technology) and v.3.4 software kits; Model CORE Radiology: The Volcano s5/s5i and CORE Series Intravascular Imaging and Pressure System is used for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2856-2015·2015-07-29

    Marine Harvest Recalls Raw Chilean Salmon Due to Listeria Risk

    Marine Harvest is recalling raw, fresh, farmed Chilean Atlantic salmon fillets due to potential Listeria monocytogenes contamination. The affected product was distributed in California, Arizona, and Nevada.

    Product
    Raw, Fresh, Farmed Chilean Atlantic Salmon -Atl Fs Sal Chilean Fill Tr D 3-4 lbs 40lbs -Atl Fs Sal Chilean Fill Deep Skinned Tr E 3-4 lbs 10LBS -Atl Fs Sal Chilean Fill Tr E 3-4 lbs 40lbs -Chilean Fresh Atl Trim D 1-6 Factory 40lbs -Chilean Fresh Atl Factory 1-6 SK off…
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2116-2015·2015-07-29

    FDA Recalls Sterile Augmentation Kits with Compromised Devon Light Gloves

    The FDA is recalling 144 sterile Augmentation Kits containing Devon Light Gloves due to splits or holes that compromise sterility. The affected kits were distributed worldwide.

    Product
    Augmentation Kit , Sterile-.Kits containing the Devon Light Glove Catalog Number/Description 573732 7620-CWA Augmentation Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2107-2015·2015-07-29

    FDA Recalls Sterile Delivery Kits Containing Defective Devon Light Gloves

    The FDA is recalling sterile delivery and C-section kits containing Devon Light Gloves with splits or holes that compromise sterility.

    Product
    Delivery/C-Section, Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description: 56479 7335-SMC C-Section Kit 31404851 7382-OTO2 Delivery Kit 52000076E 7339-ES C-SECTION DELUXE PACK 52000082E 7335-HUV DELIVERY KIT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V473000·2015-07-28

    Altec Recalls 2006-2015 Aerial Devices Due to Outrigger Interlock Defect

    Altec Industries is recalling 2,514 aerial devices from 2006-2015 because the outrigger interlock system may fail to detect proper deployment, risking boom instability and injury.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V477000·2015-07-28

    Newmar Recalls Toy Haulers Due to Unprotected Fuel System Fire Risk

    Newmar is recalling specific All Star and Canyon Star toy haulers because unprotected plastic wrap around the fuel system could burn if exposed to an ignition source.

    Product
    NEWMAR — NEWMAR ALL STAR, CANYON STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V470000·2015-07-28

    Chrysler Recalls 2015 Chrysler 200 Vehicles for Electrical Connector Defect

    Chrysler is recalling 77,971 model year 2015 Chrysler 200 vehicles because a defective electrical connector may cause intermittent power failures, potentially leading to the vehicle stalling without warning.

    Product
    CHRYSLER — CHRYSLER 200
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V468000·2015-07-27

    Chrysler Recalls 2015 Ram 4500 and 5500 Trucks for Suspension Defect

    Chrysler is recalling 199 model year 2015 Ram 4500 and 5500 pickup trucks due to a front suspension weld defect that may reduce vehicle stability and increase crash risk.

    Product
    RAM — RAM 5500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V462000·2015-07-24

    Forest River Recalls 2007-2015 Glaval Bus Titan II for Electrical Fire Risk

    Forest River is recalling 2007-2015 Glaval Bus Titan II vehicles due to a misrouted electrical cable that may cause a loose connection or arching, increasing the risk of a vehicle fire.

    Product
    GLAVAL BUS — GLAVAL BUS TITAN II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·104-2015·2015-07-23

    Brown Packing Recalls Veal Trimmings Due To Possible E. Coli Contamination

    Brown Packing Company is recalling raw veal trimmings that may be contaminated with E. coli O157:H7 and non-O157 STEC. No illnesses have been reported.

    Product
    Brown Packing Recalls Veal Products Due To Possible E. Coli Contamination
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-1236-2015·2015-07-22

    Kremers Urban Recalls Nitroglycerin Patches Due to Impurity Failure

    Kremers Urban Pharmaceuticals is recalling Nitroglycerin Transdermal Systems because they failed impurity specifications during stability testing.

    Product
    Nitroglycerin Transdermal System 0.2 mg/hr (10 cm2), For Transdermal Use Only, 30 Systems (patches) per box, Rx Only, Manufactured for: Kremers Urban Pharmaceuticals Inc., Princeton, NJ, 08540, USA, By LTS Lohmann Therapie Systeme AG, Anderach, Federal Republic of Germany, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2060-2015·2015-07-22

    Zimmer Recalls ZNN Antegrade Femoral Nail Due to Potential Denting

    Zimmer, Inc. is recalling eight ZNN Antegrade Femoral Nail units because a single distributed unit may have been dented, posing a risk of implant fatigue.

    Product
    ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Food)·F-2852-2015·2015-07-22

    Dr. Praeger's Gluten Free Veggie Burgers Recalled for Undeclared Soy

    Ungar's Food Products is recalling Dr. Praeger's Gluten Free California Veggie Burgers because they contain undeclared soy.

    Product
    Dr. Praeger's California Veggie Burgers Gluten Free 11 oz. Manufactured by Dr. Praeger's Sensible Foods Elmwood Park, NJ 07047 www.drpraegers.com Made in the USA UPC 080868000602
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2063-2015·2015-07-22

    Elekta MOSAIQ Oncology Software Recalled for Incorrect Stereotactic Field Size

    Elekta is recalling MOSAIQ Oncology Information System software due to a defect that sends incorrect field sizes to treatment machines for stereotactic plans using cones.

    Product
    MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be used wherever radiotherapy and/or chemotherapy are prescribed.
    Category
    Medical Device
    Distribution
    13 states