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.

22976–23000 of 50430

  • HighFDA (Devices)·Z-2252-2020·2020-06-10

    FDA Recalls Multifire VersaTrack Auto Suture Hernia Stapler Due to Assembly Error

    The FDA is recalling 12,610 units of the Multifire VersaTrack Auto Suture Hernia Stapler because a manufacturing error may cause staples to fail to advance properly.

    Product
    Multifire VersaTrack Auto Suture Hernia Stapler, 4.0mm, Part No. 174021 - Product Usage: has application in endoscopic general surgery procedures for fixation of mesh in the repair of hernial defects and in other surgical specialties for approximation of tissue(s).
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2242-2020·2020-06-10

    Beckman Coulter Access Thyroglobulin Antibody II Recalled for Biotin Interference

    Beckman Coulter is recalling Access Thyroglobulin Antibody II assays because biotin can cause significant result bias.

    Product
    Beckman Coulter ACCESS Immunoassay Systems, Access Thyroglobulin Antibody II, REF A32898 (UDI: 15099590202910) for use with the Access Family of Immunoassay Systems including: Access 2, UniCel DxI 600, UniCel DxI 800, UniCel DxC 600i, UniCel DxC 660i, UniCel DxC 680i, UniCel…
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-2202-2020·2020-06-10

    Agfa DR 800 X-Ray System Recalled for Dose Calculation Error

    Agfa N.V. is recalling 13 DR 800 digital radiography systems because a software error may cause incorrect dose calculations during specific fluoroscopic exams.

    Product
    AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic, Type number: 6010/200 - Product Usage: DR 800: Agfa s DR 800 system is indicated for performing dynamic imaging examinations (fluoroscopy and/or rapid sequence) of the following anatomies/procedures: positioning…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2193-2020·2020-06-10

    Baxter Gambro Cartridge Blood Set Recalled for Tubing Disconnection Risk

    Baxter Healthcare is recalling Gambro Cartridge Blood Sets due to a potential tubing disconnection hazard during hemodialysis treatment.

    Product
    Gambro Cartridge Blood Set Prime Line - Product Usage: is intended for single use in a hemodialysis treatment using Dialysis Delivery Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2179-2020·2020-06-10

    FDA Recalls Sterile Custom Surgical Packs from Unregistered Facility

    American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered by the FDA.

    Product
    Sterile Custom Packs to be used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2230-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out post-operatively.

    Product
    Vital MIS Spinal Fixation system implants CANN BL POLY EXT 8.5X50MM, Item Number 811M8550 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2246-2020·2020-06-10

    Hill-Rom Centrella Smart+ Bed Recall for Alert System Failure

    Hill-Rom is recalling 4,381 Centrella Smart+ Beds because the Bed Exit System may fail to send remote alerts to the nurse call system under specific conditions.

    Product
    Centrella Smart+ Bed, Catalog Number P7900
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0986-2020·2020-06-10

    Plucker's Wing Sauce Recalled for Undeclared Soy and Wheat

    Zilks Foods is recalling Plucker's Wing Bar World Famous Wing Sauce Baker's Gold due to potential undeclared soy and wheat.

    Product
    Plucker's Wing Bar World Famous Wing Sauce Baker's Gold 12 FL OZ. (355 mL) packaged in a glass bottle
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2176-2020·2020-06-10

    FDA Recalls Sterile Custom Surgical Packs Due to Unregistered Facility

    American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered with the FDA.

    Product
    Sterile Custom Packs to be used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2227-2020·2020-06-10

    Zimmer Biomet Recalls Vital MIS Spinal Fixation Implants Due to Locking Issues

    Zimmer Biomet is recalling Vital MIS Spinal Fixation system implants because reports indicate the extended tab screws may not lock adequately, causing the closure top to back out after surgery.

    Product
    Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 7.5X55MM, Item Number 810M7555 - Product Usage: are non-cervical spinal fixation devices intended for posterior pedicle screw fixation, posterior hook fixation, or anterolateral fixation. Pedicle screw fixation is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2198-2020·2020-06-10

    Inpeco FlexLab Augomation System Recalled for Potential Sample Dilution

    Inpeco S.A. is recalling 71 FlexLab Augomation Systems because a firmware error may dilute primary sample tubes with distilled water, potentially causing discrepant patient results.

    Product
    FlexLab Augomation System using the Aliquoter Module (Inpeco P/N FLX-212) The systems consolidate multiple Analytical instruments into a unified workstation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0993-2020·2020-06-10

    Plucker's Wing Sauce Recalled for Undeclared Soy and Wheat

    Zilks Foods is recalling 528 bottles of Plucker's Wing Bar Vampire Killer sauce in Texas and Louisiana due to potential undeclared soy and wheat.

    Product
    Plucker's Wing Bar World Famous Wing Sauce Vampire Killer 12 FL OZ. (355 mL) packaged in a glass bottle
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0989-2020·2020-06-10

    Plucker's Wing Sauce Recalled for Potential Undeclared Milk and Soy

    Zilks Foods is recalling Plucker's Wing Bar World Famous Wing Sauce Hallelujah 12 FL OZ. bottles due to potential undeclared milk and soy allergens.

    Product
    Plucker's Wing Bar World Famous Wing Sauce Hallelujah 12 FL OZ. (355 mL) packaged in a glass bottle
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·20V338000·2020-06-09

    Highland Ridge RV Recalls 2020 Trailers Due to Window Glass Detachment Risk

    Highland Ridge RV is recalling 80 units of 2020 Ridge, Open Range, and Silverstar trailers because window glass may detach and become a projectile.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW MESA RIDGE, OPEN RANGE, SILVERSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V339000·2020-06-09

    2020 Thor Motor Coach motorhome frameless windows may detach while driving

    Thor Motor Coach is recalling certain 2020-2021 motorhomes because the adhesive bond in frameless windows may fail, allowing the glass to detach and become a projectile hazard while the vehicle is in motion.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH AXIS, COMPASS, DELANO, GEMINI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V336000·2020-06-09

    Jayco Recalls 2020 Recreational Vehicles Due to Window Glass Detachment Risk

    Jayco is recalling 2020 Eagle, Jay Flight, and other models because window glass may detach and become a projectile.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER EAGLE, JAY FLIGHT, EAGLE HT, NORTH POINT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V333000·2020-06-09

    Lion Recalls 2012-2020 School Buses for Seat Belt Anchor Defect

    Lion Electric Company is recalling 2012-2020 Lion 360 and Lion C school buses because the driver's seat belt anchor may be attached with incorrect hardware, potentially compromising safety in a crash.

    Product
    LION — LION 360, LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E034000·2020-06-08

    Maxon Lift Gates Recalled for Non-Compliant License Plate Light

    Maxon Lift Corp. is recalling specific lift gates where the license plate light may aim rearward, failing federal safety standards and increasing crash risk.

    Product
    STRUCTURE:BODY:HATCHBACK/LIFTGATE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V327000·2020-06-05

    Class C Motorhome Manual Error Increases Rollaway Risk for 2019–2021 Models

    Jayco is recalling certain 2019–2021 Class C motorhomes because the Operator's Manual contains incorrect information about the automatic parking function, which could lead to unintended vehicle movement or rollaway.

    Product
    ENTEGRA — ENTEGRA, JAYCO QWEST, MELBOURNE, MELBOURNE PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V325000·2020-06-04

    Land Rover Recalls 2016 Range Rover Models for Door Latch Defect

    Jaguar Land Rover is recalling 2016 Range Rover and Range Rover Sport vehicles because a previous repair may have failed, allowing the left door to remain unlatched.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V326000·2020-06-04

    Honda Recalls 2019 Clarity Vehicles Due to Rear Seat Belt Defect

    Honda is recalling 2019 Clarity Fuel Cell, Electric, and Plug-in Hybrid vehicles because the rear seat belt locking mechanism may not function as intended, increasing injury risk in a crash.

    Product
    HONDA — HONDA CLARITY FUEL CELL, CLARITY PLUG-IN HYBRID, CLARITY ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20749·2020-06-04

    Tim Trading Recalls Emori Wintergreen Essential Oil Due to Packaging Defect

    Tim Trading is recalling Emori Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Emori Wintergreen 100% Pure Essential Therapeutic Grade Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide