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.

21226–21250 of 50426

  • HighFDA (Devices)·Z-0920-2021·2021-02-03

    OmnIlife Science Recalls Hip Replacement Liners Due to Oxidation Limits

    OmnIlife Science is recalling three units of SERF Novae Dual Mobility Cup Inserts because they exceed acceptable oxidation limits, potentially increasing wear rates and the need for revision surgery.

    Product
    SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-25128
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0899-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk

    Respironics is recalling 481 V60 Ventilators due to potential backup battery failures caused by over-discharge or extended storage without AC power.

    Product
    Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0890-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk

    Respironics is recalling 534 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.

    Product
    Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0913-2021·2021-02-03

    Philips Respironics V60 Plus Ventilator Recall Due to Navigation Ring Malfunction

    The FDA is recalling the Philips Respironics V60 Plus Ventilator because its navigation ring may become inoperative or operate intermittently, potentially causing ventilator parameter values to change erratically during setup or adjustment.

    Product
    Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0898-2021·2021-02-03

    Philips Respironics V60 Plus Ventilator Recalled for Battery Failure Risk

    Respironics is recalling 702 V60 Plus Ventilators worldwide because the backup battery may fail if over-discharged or stored without AC power.

    Product
    Philips Respironics V60 Plus Ventilator Part Number 1138747 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V045000·2021-02-03

    Royal Enfield Recalls 2018-2020 Motorcycles for Brake Caliper Corrosion

    Royal Enfield is recalling 2018-2020 Continental GT 650 and Interceptor 650 motorcycles because road salt may corrode brake calipers, potentially reducing braking performance.

    Product
    ROYAL ENFIELD — ROYAL ENFIELD INTERCEPTOR 650, CONTINENTAL GT 650
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E008000·2021-02-03

    Bigfoot Truck Campers Recalled for Potential Gas Leak Risk

    Bigfoot Industries is recalling specific 1500 and 2500 Series truck campers because a saddle valve bolt may be overtightened, damaging the seal and causing a gas leak that increases fire risk.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0218-2021·2021-02-03

    Weis Quality Cookies and Cream Ice Cream Recalled for Metal Contamination

    Weis Markets is recalling 10,869 containers of Cookies and Cream Ice Cream because the product may contain metal foreign objects.

    Product
    Weis Quality Cookies and Cream Ice Cream (48oz). Packaged in a squround paper container with a UPC of 041497-01253.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0912-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects

    Respironics is recalling 216 V60 Ventilators because the navigation ring may fail or cause erratic parameter changes.

    Product
    Philips Respironics V60 Ventilator Part Number 1076717 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0902-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects

    Respironics is recalling 2,137 V60 Ventilators because the navigation ring may malfunction or cause erratic parameter changes.

    Product
    Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0917-2021·2021-02-03

    Philips Respironics V680 Ventilator Recalled for Navigation Ring Defects

    Respironics is recalling 3,453 V680 ventilators worldwide because the navigation ring may fail or cause erratic parameter changes.

    Product
    Philips Respironics V680 Ventilator Part Number 850011 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0893-2021·2021-02-03

    Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk

    Respironics is recalling 3,213 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.

    Product
    Philips Respironics V60 Ventilator Part Number R1076709 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0908-2021·2021-02-03

    Philips Respironics V60 Ventilator Recall for Navigation Ring Issues

    Respironics is recalling 3,752 V60 Ventilators worldwide due to potential navigation ring malfunctions that may cause erratic parameter changes or inoperability.

    Product
    Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1766-2020·2021-02-03

    Philips Telemetry Transceiver Recall for Heart Rate Display Failure

    Philips is recalling 21,672 telemetry transceivers because they may fail to display heart rates or generate alarms when used with specific Patient Information Center software.

    Product
    TRx4851A 2.4 GHz IntelliVue Tele TRX, Model Number 862231; Includes Service Numbers 453564052401, 453564052411, 453564052441, 453564052451, 453564166851, 453564166861
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-02022021-01·2021-02-02

    Raw Ground Beef Alert: Possible E. Coli O157:H7 Contamination

    USDA FSIS issued a public health alert for raw ground beef sold in Sandwich, Illinois, due to possible E. coli O157:H7 contamination. Consumers should discard or return the product.

    Product
    FSIS Issues Public Health Alert for Raw Ground Beef Product Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21V039000·2021-02-01

    Micro Bird Recalls G5 Buses Due to Wiring Fire Risk

    Micro Bird is recalling 2013-2021 G5 school and transit buses because damaged electrical wiring behind the driver's seat may cause a short circuit or fire.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V038000·2021-02-01

    2021 Volkswagen Jetta front seat bolts missing, increasing crash injury risk

    Volkswagen is recalling 2021 Jetta and Tiguan vehicles because bolts may be missing from front seat tracks. Missing bolts allow seats to move freely, increasing the risk of injury in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E006000·2021-02-01

    Putco Recalls Nitro-Lux LED Headlamp Bulbs for Excessive Glare

    Putco is recalling specific Nitro-Lux LED headlamp bulbs because they may cause excessive glare to oncoming drivers, increasing crash risk.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V036000·2021-02-01

    Micro Bird Recalls G5 Buses Due to Wiring Fire Risk

    Micro Bird is recalling 2014-2021 G5 School and Transit Buses because damaged electrical wiring behind the driver's seat could cause a short circuit and fire.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V032000·2021-01-29

    Mercedes-Benz Recalls C-Class Models for Front Seat Belt Retraction Issue

    Mercedes-Benz is recalling 2017-2021 C300, AMG C43, and AMG C63 vehicles because front seat belts may not fully retract, potentially discouraging use and increasing crash injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, AMG C43, AMG C63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V030000·2021-01-28

    Autocar Xpeditor Seat Belt Harness Defect May Cause Engine Stall

    Autocar is recalling certain 2018-2021 Xpeditor vehicles because the seat belt harness may chafe and short circuit the engine, causing unexpected stalling that could lead to crashes.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0882-2021·2021-01-27

    Biomet Recalls A.L.P.S. Clavicle Plating System Due to Drill Fracture Risk

    Biomet is recalling 174 A.L.P.S. Clavicle Plating Systems because instruments may cold weld, preventing disassociation and increasing the chance of drill fracture.

    Product
    A.L.P.S. Clavicle Plating System, Plate, Fixation, Bone, Item Number 233500004 - Product Usage: indicated for fixation of fractures, osteotomies and non-unions of the clavicle including osteopenic bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide