The Recall Desk

Hazard

Injury recalls

1,366 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,366
Critical
6
Severe
415
Most recent
2026-09-03

Of the 1,366 injury recalls we have scored against our rubric, 6 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 415 (30%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all injury recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

351–375 of 1366

  • SevereNHTSA·20V154000·2020-03-18

    Bentley Recalls Bentayga Vehicles Due to Third-Row Seat Belt Defect

    Bentley is recalling 2018-2020 Bentayga vehicles with third-row seats because the upper seat belt attachment may detach in a crash, increasing injury risk.

    Product
    BENTLEY — BENTLEY BENTAYGA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V152000·2020-03-18

    BMW Recalls X3 and X4 Models for Instrument Panel Casing Defect

    BMW is recalling 2018-2020 X3 and 2019-2020 X4 vehicles because the instrument panel casing may not be tightened properly, posing an injury risk during air bag deployment.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20088·2020-03-12

    Kichler Recalls 52-inch LED Ceiling Fans Due to Blade Detachment Hazard

    Kichler Lighting is recalling 52-inch LED ceiling fans because the arms holding the blades can detach, posing an injury risk. No injuries have been reported.

    Product
    Kichler 52-inch LED Indoor Ceiling fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V115000·2020-02-27

    Altec Recalls 2019 Aerial Devices Due to Fastener Failure Risk

    Altec Industries is recalling 238 specific 2019 aerial devices because high-strength fasteners securing the pedestal to the turntable may fail, potentially causing the pedestal to separate.

    Product
    ALTEC — ALTEC LR760-E70, LR758, LR756, LR760
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V113000·2020-02-26

    Thomas Built Buses Saf-T-Liner C2 Recall for Exterior Light Failure

    Daimler Trucks North America is recalling 2017-2020 Thomas Built Buses Saf-T-Liner C2 school buses because the exterior warning lights and stop sign may fail, increasing injury risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20076·2020-02-20

    Browning Recalls Leather Pistol Holsters Due to Firearm Safety Hazard

    Browning is recalling approximately 1,265 leather pistol holsters because the design can inadvertently change the firearm's safety switch position, posing an injury risk.

    Product
    Browning Leather Pistol Holsters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1116-2020·2020-02-19

    Teleflex Recalls Rusch Greenlite Laryngoscope Blades Due to Breakage Reports

    Teleflex Medical is recalling Rusch Greenlite Single-Use Metal Laryngoscope Blades because they may break at a welded joint during setup or use.

    Product
    Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V084000·2020-02-13

    Heartland Recalls 2020 Fifth Wheel Trailers Due to Smoke Detector Placement

    Heartland is recalling 487 fifth wheel trailers because a smoke detector may be incorrectly located in the bedroom, potentially delaying fire warnings.

    Product
    HEARTLAND — HEARTLAND BIGHORN TRAVELER, ELKRIDGE, MILESTONE, PIONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0976-2020·2020-02-12

    Cook Inc. Recalls Sof-Flex Ureteral Stent Sets Due to Loading Error

    Cook Inc. is recalling 13,388 Sof-Flex Multi-Length Ureteral Stent Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient.

    Product
    Sof-Flex Multi-Lenqth Ureteral Stent Set, Global Product No. G14773 G15000 G14867 G14951 G17852
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0974-2020·2020-02-12

    Cook Inc. Recalls Kwart Retro-Inject Ureteral Stent Sets

    Cook Inc. is recalling Kwart Retro-Inject Ureteral Stent Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.

    Product
    Kwart Retro-Inject Ureteral Stent Set, Global Product No. G15016 G14836 G14885 G14887 G17151
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0964-2020·2020-02-12

    Cook Inc. Recalls Wire Guide Due to Incorrect Loading Risk

    Cook Inc. is recalling 13,388 Wire Guide units because they may be incorrectly loaded, causing the stiff tip to be introduced into patients instead of the flexible tip.

    Product
    Wire Guide, Guidewire, Global Product Number G14326
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0969-2020·2020-02-12

    Cook Percutaneous Pigtail Nephrostomy Set Recalled for Wire Guide Loading Error

    Cook Inc. is recalling Percutaneous Pigtail Nephrostomy Sets because the wire guide may be incorrectly loaded, causing the stiff tip to be introduced into the patient instead of the flexible tip.

    Product
    Percutaneous Pigtail Nephrostomy Set , Global Product No. G14094 G14095 G14899 G14329
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20E005000·2020-02-07

    Ferrara Recalls Pelican Flashlights Due to Battery Explosion Risk

    Ferrara Fire Apparatus is recalling Pelican Flashlights models 9410 and 9415 supplied with emergency vehicles because the battery pack may explode while charging.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V025000·2020-01-17

    Isuzu and Chevrolet Trucks Recalled for Seat Belt Webbing Defect

    Isuzu and Chevrolet trucks are being recalled because a manufacturing issue may prevent the seat belt webbing locking mechanism from properly restraining occupants.

    Product
    ISUZU — ISUZU, CHEVROLET NPR HD, NPR, NQR, NRR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0782-2020·2020-01-15

    Siemens Cios Alpha Mobile X-Ray System Recalled for C-Arm Holder Crack

    Siemens Medical Solutions is recalling Cios Alpha mobile X-ray systems because a crack in the C-arm holder could compromise stability and lead to injury.

    Product
    Cios Alpha, Model Number 10308191; mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical application
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0330-2020·2019-12-18

    Breakstones Cottage Cheese Recalled for Potential Plastic and Metal Contamination

    Kraft Heinz is recalling Breakstones 4% Milkfat Small Curd Cottage Cheese due to the potential presence of red plastic and metal pieces introduced during production.

    Product
    Breakstones 4% Milkfat Small Curd Cottage Cheese, in 24 oz. Plastic Tub, with UPC 0 21000 12284 4, 12 packages per case
    Category
    Food
    Distribution
    Distributed nationwide