The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

39076–39100 of 50506

  • HighFDA (Drugs)·D-693-2015·2015-04-29

    Attix Pharmaceuticals Recalls Fulvestrant API Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Fulvestrant active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.

    Product
    Fulvestrant active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-846-2015·2015-04-29

    Attix Pharmaceuticals Recalls Podophyllum Resin Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Podophyllum Resin active pharmaceutical ingredient due to potential penicillin cross-contamination from inadequate facility separation.

    Product
    Podophyllum Resin active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-669-2015·2015-04-29

    Attix Pharmaceuticals Recalls Exemestane API Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Exemestane active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging. The product was distributed nationwide to compounding pharmacies and research organizations.

    Product
    Exemestane active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1499-2015·2015-04-29

    Wright Medical Recalls Crosscheck Plating System Due to Specification Defects

    Wright Medical Technology is recalling 151 units of the Crosscheck Plating System because dimensional specifications are out of tolerance, posing a risk of intraoperative malfunction.

    Product
    CROSSCHECK(R) Plating system, Utility Plate, 7-Hole, REF CCP-UTN7. Orthopedic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-664-2015·2015-04-29

    Attix Pharmaceuticals Recalls Etodolac Due to Penicillin Cross-Contamination Risk

    Attix Pharmaceuticals is recalling Etodolac active pharmaceutical ingredient due to potential penicillin cross-contamination during repackaging.

    Product
    Etodolac active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front Street East, Unit 801, Toronto, Ontario M5A 4N3, Canada
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·15V250000·2015-04-28

    Ford Recalls 2013-2015 Fusion, MKZ, and Edge for Steering Bolt Corrosion

    Ford is recalling specific 2013-2015 Fusion, Lincoln MKZ, and 2015 Edge vehicles because road salt may corrode steering bolts, potentially causing a loss of power steering assist.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V247000·2015-04-27

    Spartan Recalls Utilimaster Vans Due to Reversed Backup Camera Images

    Spartan Motors is recalling 2012-2015 Utilimaster Walk-in vans and truck bodies because the backup camera may display reversed images, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN, TRUCK BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·059-2015 expansion·2015-04-27

    Corn Maiden Foods Recalls Beef and Pork Products for Undeclared Soy Allergen

    Corn Maiden Foods, Inc. is expanding a recall of beef and pork products due to misbranding and an undeclared soy allergen. No adverse reactions have been reported.

    Product
    Corn Maiden Foods, Inc. — Corn Maiden Foods, Inc. Recalls Beef and Pork Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·15V248000·2015-04-27

    Ford Recalls 2015 Lincoln MKZ for Excessive Parking Light Output

    Ford is recalling 21,435 2015 Lincoln MKZ vehicles because parking lights may not dim correctly when headlights are on, potentially blinding oncoming traffic.

    Product
    LINCOLN — LINCOLN MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·069-2015·2015-04-24

    Alpine Sausage Kitchen Recalls Beef and Pork Sausages for Undeclared Soy

    Alpine Sausage Kitchen is recalling approximately 3,350 pounds of beef and pork sausage products because they contain soy, a known allergen, that is not declared on the label.

    Product
    Alpine Sausage Kitchen Recalls Beef And Pork Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1947-2015·2015-04-22

    Polar Corp. Recalls Stop & Shop Orange Mango Sparkling Water for Undeclared Walnuts

    Polar Corp. is recalling Stop & Shop Clear Splash Orange Mango sparkling water because it contains undeclared walnuts, a major allergen.

    Product
    Stop & Shop Clear Splash Orange Mango, 1 liter plastic bottle Flavored Sparkling Water Beverage Distributed by Foodhold U.S.A., LLC Landover, MD 20785 UPC Codes: 6-882677-14066
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1449-2015·2015-04-22

    Hansen Medical Recalls Magellan Robotic Systems Due to Catheter Retraction Defect

    Hansen Medical is recalling 19 Magellan Robotic Systems because the catheter may fail to stop retracting when the control button is released.

    Product
    Magellan Robotic System; Model No(s). 11132 and 11139. A steerable catheter control system used at clinical sites.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1945-2015·2015-04-22

    ReNew Life Formulas Recalls Multi-Plus Vitamins Due to Gluten Mislabeling

    ReNew Life Formulas is recalling PureLife Naturals Adult Multi-Plus vitamins because labels claim 'no wheat' and 'no gluten' but the products contain gluten or wheat.

    Product
    PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle
    Category
    Food
    Distribution
    51 states
  • HighFDA (Food)·F-1998-2015·2015-04-22

    Culinary Masters Seasoning Recalled for Undeclared Peanuts in Cumin

    Gourmet Foods International is recalling Culinary Masters Seasoning Ted's Butcherblock because the cumin ingredient contains undeclared peanuts.

    Product
    Culinary Masters, SEASONING TEDS BUTCHERBLOCK, Net Wt. 7 lbs. Distributed by Atlanta Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-1974-2015·2015-04-22

    Cajun Seafood Seasoning Recalled for Undeclared Peanuts in Cumin

    Gourmet Foods International is recalling Joe Paati's Cajun Seafood Seasoning because the cumin ingredient contains undeclared peanuts.

    Product
    Joe Paatis, CAJUN SEAFOOD SEASONING, 3.5oz., Joe Pattis.com 524 South B Street, Pensacola, FL 32501.
    Category
    Food
    Distribution
    16 states
  • HighNHTSA·15V240000·2015-04-22

    Toyota Recalls 2015 Sienna Minivans Due to Trim Panel Clip Defect

    Toyota is recalling 387 model year 2015 Sienna minivans because a reused trim panel clip may detach during airbag deployment, posing an injury risk to occupants.

    Product
    TOYOTA — TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1441-2015·2015-04-22

    GE Healthcare Recalls Improperly Installed Ceiling Suspended Radiation Shields

    GE Healthcare is recalling 797 ceiling-suspended pendent systems for radiation shields and surgical lamps due to improper installation. One incident of a shield falling and causing a minor injury has been reported.

    Product
    Kenex Radiation Shield installed with GE Healthcare Interventional, Surgery, CT and X-Ray Imaging systems.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1977-2015·2015-04-22

    Culinary Masters BBQ Coffee Spice Blend Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters BBQ Coffee spice blend because cumin used in the product contained undeclared peanuts.

    Product
    Culinary Masters, SPICE BLEND BBQ COFFEE, 30 lbs., Distributed by Gourmet Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-1987-2015·2015-04-22

    Culinary Masters Cajun Seafood Spice Blend Recalled for Undeclared Peanuts

    Gourmet Foods International is recalling Culinary Masters Cajun Seafood Spice Blend because the cumin ingredient contains undeclared peanuts.

    Product
    Culinary Masters, MASTERS CAJUN SEAFOOD SPICE BLEND, Net Wt. 20 oz. and 7 lbs., Distributed by Atlanta Foods International, Atlanta, GA 30303.
    Category
    Food
    Distribution
    16 states
  • HighFDA (Devices)·Z-1451-2015·2015-04-22

    Baxter SIGMA Spectrum Infusion Pump Software Recall for Dose Display Discrepancy

    Baxter is recalling SIGMA Spectrum Infusion Pump software due to a discrepancy between Master Drug Library settings and pump display, which may cause therapy delays or unintended delivery rates.

    Product
    Master Drug Library Software version 8.0, Product Code 35723V080, to be used with SIGMA Spectrum Infusion System (Pump) version 8.0, Product Code 35700BAX2 The SIGMA Spectrum Infusion Pump with Master Drug Library (MDL) is intended to be used for the controlled…
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-1442-2015·2015-04-22

    Baylis Medical Recalls ProTrack Microcatheter Due to Circumferential Shaft Defects

    Baylis Medical Corp is recalling two lots of ProTrack Microcatheters due to potential circumferential defects along the device shaft.

    Product
    ProTrack Microcatheter; Product Usage: The ProTrack Microcatheter is a sterile, single use device intended to be used as a standard infusion wire or as an exchange guide for exchanging guidewires.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1443-2015·2015-04-22

    Bard PICC and Dialysis Catheter Kits Recalled for Scalpel Injury Risk

    Bard Access Systems is recalling PICC and dialysis catheter kits containing Safe-Cut Safety Scalpels due to the potential for inadvertent scalpel stick injuries.

    Product
    Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter kits containing Safe-Cut Safety Scalpels.
    Category
    Medical Device
    Distribution
    Distributed nationwide