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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32576–32600 of 40325

  • ModerateFDA (Devices)·Z-2019-2015·2015-07-15

    Stradis Healthcare Recalls Abdominal Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling Abdominal Packs and Abdom Packs because they contain Devon Light Gloves, a component recalled by Medtronic.

    Product
    Abdominal Pack and Abdom Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2012-2015·2015-07-15

    Stradis ACL Pack Recalled Due to Component Glove Recall

    Stradis Healthcare is recalling ACL Packs containing Devon Light Gloves because the manufacturer, Medtronic, is recalling the glove component.

    Product
    ACL Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2017-2015·2015-07-15

    Stradis Healthcare Recalls Bariatric Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling Bariatric Packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall by Medtronic.

    Product
    Bariatric Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1995-2015·2015-07-15

    Stradis Vein Surgery Packs Recalled Due to Component Issue

    Stradis Healthcare is recalling 55 vein surgery packs because they contain a Devon Light Glove component subject to a separate recall by Medtronic.

    Product
    Vein Pack, Vein Treatment II Pack, Vein Brunswick Pack, Vein No Lidocaine Pack, Vein Ablation Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2008-2015·2015-07-15

    Stradis Mississippi Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Mississippi Packs containing Devon Light Gloves due to a manufacturer recall of the glove component.

    Product
    Mississippi Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2015-2015·2015-07-15

    Stradis Healthcare Recalls Skin and Vein Packs Containing Recalled Gloves

    Stradis Healthcare is recalling Skin and Vein Packs because they contain Devon Light Gloves that Medtronic is recalling.

    Product
    Skin and Vein Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2044-2015·2015-07-15

    Volcano Intravascular Ultrasound System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 Intravascular Ultrasound Imaging and Pressure Systems due to a limitation in interoperability with the Philips Xper Flex Cardia system that may impact Fraction Flow Reserve calculations.

    Product
    Volcano s5i/s5ix/s5iz/CORE Intravascular Ultrasound Imaging and Pressure System; Product/Part numbers: s5i -806300-020 ; s5ix/s5iz - 807400-001; CORE - 400-0 I 00.02. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2053-2015·2015-07-15

    RTI Surgical Recalls Songer Spinal Cable System Due to Labeling Error

    RTI Surgical is recalling 25 units of the Songer Spinal Cable System because the box end label incorrectly identifies the material as Titanium instead of Stainless Steel.

    Product
    Songer Spinal Cable System, Single Cable, Crimp, Bar, Stainless Steel, Sterile. The DePuy Spine Cable System can be utilized anywhere monofilament wire has been previously found to be indicated.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2043-2015·2015-07-15

    Volcano Intravascular Ultrasound System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 intravascular ultrasound systems due to a limitation that may affect Fraction Flow Reserve calculations when connected to specific Philips monitors.

    Product
    Volcano s5/s5x/CORE Mobile Intravascular Ultrasound Imaging and Pressure System; Product/Part numbers: s5 - 804200-002 and 804200-014; s5x - 807300-001; CORE MOBILE - 400-0100.01. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2025-2015·2015-07-15

    Stradis Healthcare Recalls Shoulder Packs Containing Recalled Devon Light Gloves

    Stradis Healthcare is recalling surgical shoulder packs because they contain Devon Light Gloves that are subject to a separate manufacturer recall by Medtronic.

    Product
    Shoulder Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2007-2015·2015-07-15

    Stradis Surgical Packs Recalled Due to Medtronic Glove Component Issue

    Stradis Healthcare is recalling surgical and general surgery packs because they contain Devon Light Gloves, a component being recalled by Medtronic.

    Product
    Surgical Pack and General Surgery Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2009-2015·2015-07-15

    Stradis Face Lift Pack Recalled Due to Component Recall

    Stradis Healthcare is recalling Face Lift Packs because they contain a Devon Light Glove that is being recalled by its manufacturer, Medtronic.

    Product
    Face Lift Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2006-2015·2015-07-15

    Stradis Tummy Tuck Pack Recalled Due to Component Defect

    Stradis Healthcare is recalling Tummy Tuck Packs because they contain a Devon Light Glove component that is subject to a separate recall by Medtronic.

    Product
    Tummy Tuck Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2051-2015·2015-07-15

    Synthes Recalls Three Titanium Tibial Nail End Caps for Missing Inspection

    Synthes is recalling three units of a titanium end cap for tibial nails because they were shipped before a required internal inspection was completed.

    Product
    TITANIUM END CAP WITH T40 STARDRIVE RECESS, 0MM EXTENSION FOR TITANIUM TIBIAL NAILS-EX; Synthes Tibial Nail System EX is intended to stabilize fractures of the proximal and distal tibia and the tibial shaft; open and closed tibial shaft fractures; certain pre-and post-isthmic…
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2001-2015·2015-07-15

    Stradis Vaginal Rejuvenation Pack Recalled Due to Component Recall

    Stradis Healthcare is recalling Vaginal Rejuvenation Packs because they contain a Devon Light Glove component that Medtronic is recalling.

    Product
    Vaginal Rejuvenation Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2037-2015·2015-07-15

    Stradis Blepharoplasty Packs Recalled Due to Component Recall

    Stradis Healthcare is recalling Blepharoplasty Packs because they contain Devon Light Gloves, which are subject to a separate recall by Medtronic.

    Product
    Blepharoplasty Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2042-2015·2015-07-15

    Stradis Upper Extremity Packs Recalled Due to Component Defect

    Stradis Healthcare is recalling Upper Extremity Packs because they contain a Devon Light Glove component being recalled by Medtronic.

    Product
    Upper Extremity Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1988-2015·2015-07-15

    Allergan Recalls Expired Natrelle Breast Implant Sizers

    Allergan is recalling 9 units of expired Natrelle 410cc Re-Sterilizable Breast Implant Sizers because they were shipped to the user level.

    Product
    Natrelle Re-sterilizable Breast Implant Sizer, Size: 410 cc, Style No. MSZFX410. The product is packaged in a thermoformed tray (double sterile barrier) and enclosed in a labeled carton.
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1994-2015·2015-07-15

    Stradis Advanced Vein Care Kits Recalled Due to Component Recall

    Stradis Healthcare is recalling Advanced Vein Care kits because they contain a Devon Light Glove component recalled by Medtronic.

    Product
    Advanced Vein Care - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2004-2015·2015-07-15

    Stradis Healthcare Recalls Laser Evlt Packs Due to Component Recall

    Stradis Healthcare is recalling three Laser Evlt Packs and Laser One Leg Evlt kits because they contain a Devon Light Glove component recalled by Medtronic.

    Product
    Laser Evlt Pack and Laser One Leg Evlt - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2016-2015·2015-07-15

    Stradis Vasc Custom Kits Recalled Due to Component Recall

    Stradis Healthcare is recalling Vasc Custom Kits because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.

    Product
    Vasc Custom Kit - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide