The Recall Desk

Hazard

Instability recalls

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

What the numbers show

Total
30
Critical
2
Severe
5
Most recent
2026-08-05

Of the 30 instability recalls we have scored against our rubric, 2 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 5 (17%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all instability 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.

1–25 of 30

  • HighFDA (Devices)·Z-2805-2026·2026-08-05

    Permobil Recalls M5 Corpus Power Wheelchairs Due to Firmware Drive Inhibit Issue

    Permobil Inc. is recalling 715 M5 Corpus Power Wheelchairs (REF 120032) because firmware versions 1.27 through 1.57 lack drive inhibit logic, which may allow driving under restricted conditions and cause instability.

    Product
    M5 Corpus Power Wheelchair REF,120032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·26634·2026-07-23

    12-Drawer Fabric Dressers Recalled for Tip-Over and Entrapment Hazards

    Romorgniz 12-Drawer Fabric Dressers sold on Amazon pose tip-over and entrapment risks to children if not anchored to the wall. About 10,040 units are affected.

    Product
    Romorgniz 12-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26288·2026-02-26

    Trankerloop Baby Bath Seats Recalled Due to Drowning Risk

    Trankerloop is recalling approximately 2,380 baby bath seats because they are unstable and can tip over, posing a risk of serious injury or death from drowning.

    Product
    Trankerloop Baby Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V952000·2024-12-20

    Altec AT200A Front Axle Defect Recall for Ford E350 Chassis

    Altec is recalling AT200A devices on 2017-2024 Ford E350 chassis due to a front axle defect that may fail at high loads, increasing injury risk.

    Product
    ALTEC — ALTEC AT200A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1506-2024·2024-04-17

    Chromophare Surgical Light System recalled for insufficient mounting force

    Stryker Communications recalls Chromophare Surgical Light Systems due to insufficient mounting force that could compromise the equipment's stability in surgical environments.

    Product
    Chromophare Surgical Light System , REF CH00000001
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·23V407000·2023-06-06

    Pierce Aerial Ladder Platform Stabilizer Beam Cracks Pose Instability Risk

    Pierce is recalling certain 2016-2022 Ascendant 107' and 110' Platforms with potentially cracked galvanized stabilizer beams that could cause instability when elevated, increasing injury risk.

    Product
    PIERCE — PIERCE LADDER AND PLATFORM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22719·2022-02-03

    River Street Five-Drawer Chests Recalled for Tip-Over and Entrapment Hazards

    BFG North Carolina is recalling about 1,380 River Street Five-Drawer Chests sold at Rooms To Go from February 2019 through October 2021. The dressers are unstable if not anchored to the wall, posing tip-over and entrapment hazards that may result in death or serious injuries to children.

    Product
    River Street Five-Drawer Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22713·2021-12-16

    Karmas Far Infant Bath Seats Recalled for Drowning Hazard

    Karmas Far infant bath seats fail federal safety standards and can tip over during use, posing a drowning hazard to babies. About 900 units sold online between August 2017 and October 2021 are affected. No injuries have been reported.

    Product
    Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·21779·2021-09-09

    Burley Ballz QR Skewers Recalled Due to Fall Hazard

    Burley Design is recalling Ballz QR Skewers, which attach cargo trailers to bicycles, because the skewer can shear or bend, potentially destabilizing the trailer and bicycle and causing the rider to fall.

    Product
    Ballz QR Skewers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·21764·2021-07-22

    Bel Furniture Recalls Barrington 5-Drawer Chests for Tip-Over Hazards

    Bel Furniture is recalling about 90 Barrington 5-Drawer Chests because the dressers can tip over and trap children if not anchored to the wall. One child has already been injured when a chest tipped over.

    Product
    Barrington 5-Drawer Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1823-2020·2020-05-06

    U&I Corp. Recalls Velofix SA Cervical Cages Due to Dimensional Defects

    U&I Corp. is recalling 42 Velofix SA cervical cages because screw-hole dimensions may be out of range, posing a risk of screw pullout or instability.

    Product
    Velofix SA cervical cage, REF: TSA161207, TSA161208, TSA161209, TSA161210, TSA161407, TSA161408, TSA161409, TSA161410 - Product Usage:The device is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disk disease at one level fr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0739-2020·2020-01-01

    Ortho Clinical Diagnostics Recalls VITROS 7% BSA Diluent Due to Instability

    Ortho Clinical Diagnostics is recalling VITROS 7% BSA diluent because it may become unstable when stored in a 2mL cup for seven days.

    Product
    7% BSA (Bovine Serum Albumin), Product Code: 8262487 - Product Usage: is used to dilute samples when assay values exceed the reportable (dynamic) range using the VITROS 250/350/5,1 FS/4600 Chemistry Systems and VITROS 5600/XT 7600 Integrated Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1983-2019·2019-07-24

    Olympus Mobile Workstations Recalled for Potential Instability

    Olympus is recalling WM-NP2 and WM-DP2 mobile workstations because the control panel arm may cause the unit to fall over if a heavy monitor is attached.

    Product
    Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0714-2018·2018-03-07

    Siemens CT Table Recalled Due to Potential Bolt Loosening and Instability

    Siemens Medical Solutions is recalling SOMATOM Go.Now CT system tables because bolts may loosen, causing the table to become unstable.

    Product
    SOMATOM Go.Now computed tomography (CT) x-ray system table, Model Number: 11061618 Product Usage: Intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by these systems can be used by a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0713-2018·2018-03-07

    Siemens SOMATOM Go.Up CT Table Recall for Potential Instability

    Siemens Medical Solutions is recalling six SOMATOM Go.Up CT system tables because improperly tightened bolts may loosen, causing the table to become unstable.

    Product
    SOMATOM Go.Up computed tomography (CT) x-ray system table, Model Number: 11061628 Product Usage: Intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data. The images delivered by these systems can be used by a t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V154000·2016-03-16

    Terex Recalls Aerial Devices Due to Suspension Air Bag Defect

    Terex is recalling 2015-2016 aerial devices and digger derrick lifts because the suspension circuit can inflate air bags, lifting outriggers and increasing injury risk.

    Product
    TEREX — TEREX GENERAL 80, TM100, TM125, C5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V258000·2015-05-01

    Starcraft RV Recalls 2016 Travel Trailers with Incorrect Tire Labels

    Starcraft RV is recalling 36 model year 2016 Launch and AR-One travel trailers because Federal Certification Labels may list the wrong tire size.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE, LAUNCH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1807-2013·2013-07-31

    Etac Swift Mobil Shower Chairs Recalled for Stability Risk

    Etac is voluntarily recalling Swift Mobil shower chairs because a lost caster can cause instant instability and potential injury.

    Product
    Swift Mobil shower chair, Swift Mobil 160 shower chair, and Swift Mobil Tilt shower chair. Height adjustable four wheeled shower chairs for persons of various weights.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0810-2013·2013-02-20

    Mizuho Orthopedic Table Spar Recall Due to Possible Instability

    Mizuho OSI is recalling 869 orthopedic table spars because a failed epoxy bond could cause the aluminum plug to migrate, potentially compromising table stability.

    Product
    Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.
    Category
    Medical Device
    Distribution
    48 states
  • HighCPSC·12001·2011-10-04

    Ballard Designs Recalls Stafford Step Stools Due to Fall Hazard

    Ballard Designs is recalling about 2,500 Stafford step stools because plastic tabs on the feet make them unstable, posing a fall hazard.

    Product
    Ballard Designs "Stafford" step stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide