The Recall Desk

State

Vermont product recalls

73,576 recalls have nationwide distribution and so reach Vermont. 2,011 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total
2,011
Critical
209
Severe
531
Most recent
2026-10-21

Of the 2,011 recalls naming Vermont we have scored against our rubric, 209 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 531 (26%) are Severe.

Which agencies issued them

These figures cover only the 2,011 recalls whose distribution notice names Vermont specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

151–175 of 75587

  • HighFDA (Drugs)·N/A·2026-10-14

    Beak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination

    Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.

    Product
    Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding, 7447 Harwin Dr. Suite 111, Houston, TX 77036
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0101-2027·2026-10-14

    Avid Medical Recalls 30 DAVINCI LAP/GYN Kits for Lubricant Contamination

    Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.

    Product
    DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0090-2027·2026-10-14

    Onkos My3D Personalized Pelvic Implant Recalled for Distribution Error

    Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.

    Product
    Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0095-2027·2026-10-14

    AVID Medical Recalls 33 Endovascular Packs Due to Lubricant Contamination

    AVID Medical, Inc. is recalling 33 Endovascular Packs (Model VAPX014-04) because they may be contaminated with a lubricant used during manufacturing.

    Product
    ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0103-2027·2026-10-14

    AVID Medical Recalls Urology Kits for Potential Lubricant Contamination

    AVID Medical, Inc. is recalling 20 Urology Major kits (Model WRNM058-10) because they may be contaminated with a lubricant used during manufacturing.

    Product
    UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0082-2027·2026-10-14

    DRG Sperm Ab ELISA Recalled for Potential False Negative Results

    DRG International is recalling Sperm Ab ELISA kits due to a potential for false negative patient results. The recall covers 211 units distributed in the US and several international countries.

    Product
    Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96 well plate test);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0013-2027·2026-10-14

    Preferred Pharmaceuticals Recalls Lidocaine Ointment Due to Content Uniformity Failures

    Preferred Pharmaceuticals is recalling Lidocaine Ointment USP, 5% due to failed content uniformity specifications. The product is distributed nationwide.

    Product
    Lidocaine Ointment USP, 5% (Generic for Xylocaine), packaged in a 50 g jar, Rx only, Mfg: Taro Pharmaceuticals U.S.A., Inc., Prod# (NDC): 68788-7865-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0102-2027·2026-10-14

    AVID Medical Recalls Heart Prep Trays for Lubricant Contamination

    AVID Medical, Inc. is recalling 96 Heart Prep Trays (Model MECV97W) because they may be contaminated with a lubricant used during manufacturing.

    Product
    HEART PREP TRAY; Model/Item Number (Kit): MECV97W;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0091-2027·2026-10-14

    Onkos Surgical Recalls My3D Personalized Pelvic Implant Due to Distribution Error

    Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.

    Product
    Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0014-2027·2026-10-14

    Cipla Recalls Fosfomycin Tromethamine Due to Impurity Specification Failures

    Cipla USA, Inc. is recalling specific lots of Fosfomycin Tromethamine granules because they failed impurity and degradation specifications.

    Product
    FOSFOMYCIN TROMETHAMINE — FOSFOMYCIN TROMETHAMINE (FOSFOMYCIN TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0077-2027·2026-10-14

    Halyard Laparoscopy Comprehensive Pack II Recalled for Latex Content

    GRI Medical is recalling Halyard Laparoscopy Comprehensive Pack II kits because they contain a latex urethral catheter despite being labeled as latex-free.

    Product
    HALYARD Laparoscopy Comprehensive Pack II REF: 49332
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0100-2027·2026-10-14

    AVID Medical Recalls Plastic Trays Due to Lubricant Contamination

    AVID Medical, Inc. is recalling 28 units of EURO053 plastic trays potentially contaminated with manufacturing lubricant. The units were distributed in AZ, CA, FL, MD, NE, and TX.

    Product
    PLASTICS TRAY; Model/Item Number (Kit): EURO053;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0083-2027·2026-10-14

    Beckman Coulter Recalls DxC 500i Clinical Analyzer Modules Due to Software Error

    Beckman Coulter is recalling DxC 500i Clinical Analyzer Modules because a software issue can cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results.

    Product
    DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE, DxC 500i, Part No. C63522 2. DxC 500 AU Module, DxC 500i, Part No. C63521 3. Access 2 Module, DxC 500i, Part No. C13252
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0097-2027·2026-10-14

    Avid Medical Recalls Open Heart Kits Due to Lubricant Contamination

    Avid Medical is recalling 124 Open Heart CFH kits because they may be contaminated with a lubricant used during manufacturing.

    Product
    PACK OPEN HEART CFH; Model/Item Number (Kit): 1. UFCF004-06, 2. UFCF004-07;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0092-2027·2026-10-14

    Avid Medical Recalls Davinci Trucustom Bundles Due to Lubricant Contamination

    Avid Medical, Inc. is recalling 144 Davinci Trucustom Bundles because they may be contaminated with a lubricant used during manufacturing.

    Product
    DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064-28;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0080-2027·2026-10-14

    Limitless Cryo Spa LLC Recalls Glypto Devices for Lack of 510(k) Clearance

    Limitless Cryo Spa LLC is recalling 219 Glypto Devices and Cryo Machines because they lack FDA 510(k) clearance. The recall covers units distributed nationwide.

    Product
    Glypto Device, Glypto Cryo Machine;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0096-2027·2026-10-14

    AVID Medical Recalls Craniotomy Packs Due to Potential Lubricant Contamination

    AVID Medical, Inc. is recalling 10 Craniotomy Packs (Model WRNM035-20) because they may be contaminated with a lubricant used during manufacturing.

    Product
    CRANIOTOMY PACK; Model/Item Number (Kit): WRNM035-20;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0093-2027·2026-10-14

    AVID Medical Recalls GYN Laparoscopy Kits for Potential Lubricant Contamination

    AVID Medical, Inc. is recalling 134 GYN Laparoscopy/Laparotomy kits due to potential contamination with a manufacturing lubricant.

    Product
    GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH108-03;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0076-2027·2026-10-14

    Quantum Ops Recalls ADAPTABLE Beach Chair Surgical Patient Positioners

    Quantum Ops Inc is recalling 266 ADAPTABLE Beach Chair surgical patient positioners due to a manufacturing issue involving inadequate welds in the patient head positioning system.

    Product
    Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient positioner Model/Catalog Number: 804-33-300 (Enovis); 3105-400-030 (Stryker); internal BC-0001 / BC-0220 Software Version: N/A Product Description: Surgical beach-chair positioner that mounts to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0094-2027·2026-10-14

    Avid Medical Recalls Adult Heart Tray Shands Jacks Due to Lubricant Contamination

    Avid Medical, Inc. is recalling 59 units of Adult Heart Tray Shands Jacks (Model SHND419-08) because they may be contaminated with a lubricant used during manufacturing.

    Product
    ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0084-2027·2026-10-14

    Beckman Coulter DxC 500 AU Clinical Chemistry Analyzers Recalled for Software Error

    Beckman Coulter is recalling DxC 500 AU Clinical Chemistry Analyzers due to a software issue that may cause test units to revert to defaults without warning, potentially resulting in falsely elevated reported results.

    Product
    DxC 500 AU Clinical Chemistry Analyzers: 1. AU w/out ISE, Part No. C63519 2. AU w/ISE, Part No. C63520
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0098-2027·2026-10-14

    Avid Medical Recalls Robotic Prostatectomy Packs for Lubricant Contamination

    Avid Medical, Inc. is recalling six Robotic Prostatectomy Packs (NAMC423-11) because they may be contaminated with a manufacturing lubricant.

    Product
    ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0117-2027·2026-10-14

    LeMaitre TufTex Over-the-Wire Embolectomy Catheter Recalled for Balloon Failure

    LeMaitre Vascular, Inc. is recalling 54 TufTex Over-the-Wire Embolectomy Catheters because the balloon components may fail under pull force.

    Product
    TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0104-2027·2026-10-14

    AVID Medical Recalls Major Packs Due to Potential Lubricant Contamination

    AVID Medical, Inc. is recalling 40 Major Packs (Model NIHB0018-11) because they may be contaminated with a lubricant used during manufacturing.

    Product
    MAJOR PACK; Model/Item Number (Kit): NIHB0018-11;
    Category
    Medical Device
    Distribution
    Distributed nationwide