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.

31826–31850 of 50502

  • HighFDA (Devices)·Z-2683-2017·2017-07-19

    ICU Plum A+ Infusion Systems Recalled for Battery-Related Therapy Interruption

    ICU is recalling 363,892 Plum A+ Infusion Systems because battery issues can cause an E321 error code, potentially interrupting patient therapy.

    Product
    The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2549-2017·2017-07-19

    Matlaws Pre-Cooked Fish Squares Recalled for Undeclared Milk

    National Fish & Seafood is recalling Matlaws All Natural Panko Pre-Cooked Fish Squares because the product may contain undeclared milk.

    Product
    MATLAWS ALL NATURAL PANKO PRE COOKED FISH SQUARES 10 LB and 10/2 LB
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2692-2017·2017-07-19

    St. Jude Medical Recalls Proclaim 7 Elite Implantable Pulse Generators

    St. Jude Medical is recalling 9,529 Proclaim 7 Elite implantable pulse generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.

    Product
    Proclaim 7 Elite, Implantable Pulse Generator, REF 3662, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2712-2017·2017-07-19

    Toshiba APLIO i-series Ultrasound Systems Recalled for Incorrect Velocity Readings

    Toshiba is recalling 28 APLIO i-series diagnostic ultrasound systems because they may display incorrect velocity values when using the Continuous Trace method.

    Product
    APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 TUS AI800 diagnostic ultrasound system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2714-2017·2017-07-19

    ArjoHuntleigh Flowtron ACS900 Medical Pump Recalled for Deflation Failure

    Arjo, Inc. is recalling 40,675 Flowtron ACS900 medical pumps worldwide because the device may fail to deflate the calf garment as intended without triggering an alarm.

    Product
    ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thrombosis (DVT) in at-risk patients. The system must be used as part of a prescribed plan of car under the supervision of trained medical and/or Clinical staff.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2698-2017·2017-07-19

    Arrow Recalls EVOLUTION Pressure Injectable PICC Catheters Due to Hub Tab Detachment

    Arrow International is recalling EVOLUTION Pressure Injectable PICC catheters because the peel-away component hub tabs may prematurely detach during use.

    Product
    Arrow EVOLUTION Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombogenic Technology
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-2721-2017·2017-07-19

    ICU Medical Recalls MicroClave Extension Sets Due to Leak Risk

    ICU Medical is recalling 100 units of MicroClave extension set kits because the connection between the Female Luer and the NanoClave manifold may develop a leak.

    Product
    Kit w/3 Ext Sets, 3 Drop-In MicroClave¿ Clear. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter…
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-2550-2017·2017-07-19

    Matlaws Pre-Cooked Fish Sticks Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Matlaws All Natural Panko Pre-Cooked Fish Sticks because the product may contain undeclared milk.

    Product
    MATLAWS ALL NATURAL PANKO PRE COOKED FISH STICKS 1/10 LB and 10/2 LB
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-2472-2017·2017-07-19

    Hannaford Seafood Stuffing Recalled for Undeclared Milk Allergen

    Greencore USA is recalling Hannaford Classic Seafood stuffing due to undeclared milk. The product was distributed in Maine, New York, and Pennsylvania.

    Product
    Hannaford Classic Seafood stuffing, 10 oz. UPC 41268205097
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2727-2017·2017-07-19

    Natus Neurology Recalls Elite Obstetric Probes Due to Excessive Background Noise

    Natus Neurology is recalling 2,335 Elite Obstetric probes because excessive background noise may mask fetal heart rate and blood flow monitoring.

    Product
    Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe, Model #: X1L008, Catalog Code: NW20. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-2588-2017·2017-07-19

    NatureBox Mini Crispy Snickerdoodles Recalled for Cashew Fragment

    NatureBox is recalling Mini Crispy Snickerdoodles because a cashew fragment was found during packing, posing a potential allergen risk.

    Product
    NatureBox Mini Crispy Snickerdoodles: Cinnamon-sugar cookies made with whole wheat. Contains: Wheat, Milk and Egg.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17756·2017-07-18

    Polaris Recalls RZR 570 and RZR S 570 Off-Highway Vehicles

    Polaris is recalling about 1,160 RZR 570 and RZR S 570 vehicles because the front brake can detach, posing crash and injury hazards.

    Product
    Polaris RZR 570 and RZR S 570 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V456000·2017-07-18

    Winnebago Recalls 2015 Transit Buses for Weight Rating Compliance Issues

    Winnebago is recalling 2015 Transit Bus 28SH and 28WC models because they may exceed weight ratings when fully loaded, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRANSIT BUS28SH, TRANSIT BUS28WC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V455000·2017-07-18

    Pierce Fire Trucks Recalled for Water Pump Interlock Failure

    Pierce is recalling 2016-2017 fire trucks because a pressure switch may fail in extreme cold, preventing the water pump from operating.

    Product
    PIERCE — PIERCE ENFORCER, VELOCITY, QUANTUM, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V452000·2017-07-17

    Daimler Trucks Recalls 2018 Freightliner and Western Star Models for Tow Hook Defect

    Daimler Trucks North America is recalling 2,483 2018 Freightliner and Western Star trucks because their tow hooks may fail during recovery operations, increasing the risk of injury.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR M2 BUSINESS CLASS, 122SD, CASCADIA, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E037000·2017-07-17

    PACCAR Recalls Braden Hydraulic Recovery Winches Due to Adapter Defect

    PACCAR is recalling specific Braden Hydraulic Recovery winches because a defective ring gear adapter may cause failure under load, posing an injury risk.

    Product
    EQUIPMENT:MECHANICAL:WINCH recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V453000·2017-07-17

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Wheelchair Defect

    Daimler Trucks North America is recalling 2005-2018 Thomas Built Buses Saf-T-Liner C2 school buses because wheelchair pocket track anchorages may not secure wheelchairs in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V448000·2017-07-16

    Smart Fortwo Recall for Parking Brake Cable Lock Nut Issue

    Mercedes-Benz USA is recalling 2016 Smart Fortwo vehicles because the parking brake cable lock nut may loosen, potentially reducing the vehicle's ability to stay secured on slopes.

    Product
    SMART — SMART FORTWO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·081-2017·2017-07-14

    Custom Culinary Recalls Chicken and Beef Soup Bases Due to Misbranding

    Custom Culinary, Inc. is recalling approximately 9,444 pounds of chicken and beef soup base products due to misbranding and undeclared soy allergens.

    Product
    Custom Culinary, Inc. — Custom Culinary, Inc. Recalls Chicken and Beef Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17187·2017-07-13

    TJX Recalls Glass Beer Mugs Due to Burn and Laceration Hazards

    TJX is recalling glass beer mugs sold at HomeGoods because they can break when heated or used with hot liquids, posing burn and laceration risks.

    Product
    Glass beer mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17186·2017-07-13

    YSN Imports Recalls Refillable Propane Cylinders Due to Fire and Explosion Hazards

    YSN Imports is recalling approximately 24,000 refillable propane cylinders sold under Flame King, Little Kamper, and U-Haul brands because the connecting valve can unscrew, posing fire and explosion risks.

    Product
    Refillable propane cylinders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V440000·2017-07-13

    Jayco Recalls 2017 Jay Flight SLX Trailers for Inaccurate Weight Labels

    Jayco is recalling 2017 Jay Flight SLX travel trailers with the Rocky Mountain Package because their cargo capacity labels are inaccurate, which could lead to overloading.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
    Category
    Vehicle
    Distribution
    Distributed nationwide