Hazard

Structural Defect recalls

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

About this hazard tag

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

76–100 of 293

HighFDA (Devices)·Z-1702-2025·2025-05-07
Tibial Augment Femoral Screw Recalled for Missing Thread
Waldemar Link is recalling Tibial Augment medical devices because preassembled Femoral Augment screws are missing their threads, preventing proper fixation. The recall affects 1771 units distributed nationwide.
Product
Tibial Augment; Item Numbers: (1) 880-331/11 (Sz. 1-2 - cemented x-sm), (2) 880-331/12 (Sz. 1-2 - cemented sm), (3) 880-331/13 (Sz. 1-2 - cemented md), (4) 880-331/21 (Sz. 1-2 - cemented lg), (5) 880-331/22 (Sz. 1-2 - cemented x-lg), (6) 880-331/23 (Sz. 1-2 - cemented xx-lg), (7)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1700-2025·2025-05-07
Posterior Femoral Augment Surgical Implant with Missing Screw Thread Recalled
Waldemar Link is recalling Posterior Femoral Augment orthopedic implants distributed nationwide due to missing threads on preassembled screws. Patients should contact their surgeon immediately.
Product
Posterior Femoral Augment; Item Numbers: (1) 880-310/11 (Sz. 0 - cemented sm), (2) 880-310/21 (Sz. 0 - cemented lg), (3) 880-311/11 (Sz. 1-2 - cemented sm), (4) 880-311/21 (Sz. 1-2 - cemented lg), (5) 880-313/11 (Sz. 3-4 - cemented sm), (6) 880-313/12 (Sz. 3-4 - cemented md), (7)
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V575000·2025-04-09
2025 Jeep Wagoneer S Recalled for Defective Instrument Panel Beam
Chrysler is recalling approximately 8 units of the 2025 Jeep Wagoneer S due to an incorrect cross beam in the instrument panel that fails to comply with federal occupant crash protection standards.
Product
JEEP — 2025 JEEP WAGONEER S
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1497-2025·2025-04-09
Anesthesia Circuit Kit Flex 6 Recalled for Potential Breathing Hose Cracks
Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V580000·2025-04-09
IC Bus School Buses Recalled for Structural Reinforcement Defect
International Motors is recalling certain 2016-2026 IC Bus CESB and 2016-2021 RESB school buses due to missing or incomplete underfloor reinforcement that may compromise crash safety. Owners should contact a dealer for free inspection and installation.
Product
IC BUS — 2020 IC BUS CESB
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25208·2025-04-03
Polaris RZR Pro R and Pro R 4 recalled for ROPS fastener defect
Polaris is recalling about 910 RZR Pro R and Pro R 4 recreational off-road vehicles (2022-2025) due to missing or loose fasteners on the rollover protective structure that can fail to protect occupants in a rollover or tip-over.
Product
Model Year 2022-2025 RZR Pro R and RZR Pro R 4 Recreational Off-Road Vehicles (ROVs)
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1288-2025·2025-03-26
Smiths Medical ProPort Implantable Port Plastic Housing May Separate
The ProPort Low Profile Plastic Venous Access System is being recalled because the port housing and port reservoir may separate due to a manufacturing defect, affecting approximately 2,236 units distributed worldwide.
Product
smiths medical ProPort Low Profile Plastic Venous Access System, Silicone Catheter, 2.8mm (8.4Fr) O.D. x 1.0mm I.D., 9Fr Introducer, REF 21-4187-24
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1309-2025·2025-03-19
Aesculap Hemostatic Forceps Recalled Due to Clamp Breakage
Aesculap Inc is recalling 917,965 units of nonsterile hemostatic forceps across multiple models because the clamps can break when used beyond design specifications. No injuries have been reported.
Product
Numerous models of nonsterile hemostatic forceps: (1) REF BH100R, Carrel Artery Forceps 85MM; (2) REF BH104R, Hartmann Mosquito FCSDEL STR 100MM; (3) REF BH105R, Hartmann Mosquito FCPSDELCVD100MM; (4) REF BH108R, Micro-Halsted Forceps DEL STR125MM; (5) REF BH109R, Micro-Hals
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V753000·2025-03-11
Volvo VAH trucks recalled for seat belt anchor defects
Volvo Trucks is recalling 2019-2026 VAH trucks because the passenger seat belt anchor may fail due to inadequate floor reinforcement, preventing proper occupant restraint in crashes.
Product
VOLVO — 2019 VOLVO VAH
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V764000·2025-03-10
2018–2022 BMW X3 rear cargo rail attachment defect recall
BMW is recalling 2018–2022 X3 vehicles because rear cargo rail attachment bolts may become damaged in a rear crash, causing the rail to detach and increasing injury risk. Dealers will replace the bolts free of charge.
Product
BMW — 2020 BMW X3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V653000·2025-03-09
Peterbilt 567 and 579 Trucks: Fuel Tank Puncture Risk from Loose U-bolts
PACCAR is recalling 2021-2024 Peterbilt 567 and 579 trucks. U-bolts securing the air tank can contact and wear through the fuel tank over time. A punctured tank can leak fuel, increasing the risk of fire.
Product
PETERBILT — 2021 PETERBILT 567
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1159-2025·2025-02-26
Azurion 7 M12 Patient Tables: Fall Risk from Defective Mattress
Philips Azurion 7 M12 patient tables are recalled due to a mattress defect that could cause patients to fall. Approximately 1,837 units are affected globally.
Product
Azurion 7 M12; Catalog numbers: (1) 722078, (2) 722223, (3) 722233 (OUS ONLY).
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·25145·2025-02-20
SEJOV Five-Drawer Dressers Recalled for Tip-Over and Entrapment Hazards
About 900 SEJOV five-drawer dressers sold on Amazon from September 2023 through August 2024 are unstable if not properly anchored to a wall, posing tip-over and entrapment hazards to children. No injuries have been reported.
Product
SEJOV Five-Drawer Dressers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1166-2025·2025-02-19
Novation XLE hip implant components recalled for missing barrier layer
Exactech is recalling Novation XLE hip implant components due to absence of an Ethylene Vinyl Alcohol (EVOH) barrier layer. Patients with affected implants should contact their healthcare provider.
Product
Novation XLE Item Number / Product Description: 140-22-70 NV EHXL NTL LNR G00 22MM 140-28-50 NV EHXLNTRL LNR G0 28MM 140-28-51 NV EHXLNTRL LNR G1 28MM 140-28-52 NV EHXL NTRL LNR G228MM 140-32-51 NV EHXL NTRL LNR G132MM 140-32-52 NV EHXL NTRL LNR G232MM 140-32-53 NV EHXL N
Category
Medical Device
Distribution
22 states
HighCPSC·25123·2025-02-06
Sling Carriers Recalled for Fall Hazard Due to Safety Violations
About 18,650 sling carriers sold on Temu.com violate federal safety regulations for structural integrity and occupant retention, posing a fall hazard to babies. No injuries have been reported.
Product
Sling Carriers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·23V376000·2025-02-05
Travel trailers recalled for missing wardrobe cabinet backer board
Certain 2021-2023 Keystone Arcadia travel trailers lack a backer board behind the wardrobe cabinet, potentially allowing the slide room to extend and cause injury. Dealers will install steel brackets to secure the slide room at no cost.
Product
KEYSTONE — 2021 KEYSTONE ARCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1039-2025·2025-02-05
Knee Implant Component Recalled for Incorrect Metal Post Assembly
Zimmer, Inc. is recalling 155 units of NexGen LCCK Legacy knee implant components because the metal support post was assembled incorrectly in some units. The defective assembly could compromise implant function.
Product
NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V109000·2025-02-02
2023 Triumph Tiger Sport and Trident 660 Front Fork Caps May Detach
Front fork caps on 2023 Triumph Tiger Sport 660 and Trident 660 motorcycles may detach due to incorrectly machined threads, potentially causing loss of vehicle control and crash risk.
Product
TRIUMPH — 2023 TRIUMPH TIGER SPORT 660
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0894-2025·2025-01-22
Nuclear medicine system detector mounting safety defect
GE Healthcare is recalling certain nuclear medicine imaging systems that may have improper detector support from transport, creating a risk of detector fall and life-threatening bodily injury.
Product
GE Healthcare Discovery NM/CT 670 ES, Model/Catalog Numbers: 1) H3100XF ; System, Tomography, Computed, Emission
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0890-2025·2025-01-22
Nuclear Medicine Systems at Risk of Detector Fall During Transport
Certain GE Healthcare nuclear medicine systems were potentially transported without proper detector support, risking detector fall and life-threatening injury. Affected facilities should have their equipment inspected before clinical use.
Product
GE Healthcare Discovery NM 630, Model/Catalog Numbers: 1) 5376204-30-2, 2) H2401CF, 3) H2401CH, 4) H2401JE, 5) H3100JY; System, Tomography, Computed, Emission
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0806-2025·2025-01-15
EnVisio Patient Pad Transition Cushion surgical bed frame detachment risk
Elucent Medical is recalling the EnVisio Patient Pad Transition Cushion due to a potential safety risk of the surgical bed frame's back section detaching during use. Approximately 283 units are affected across 16 U.S. states.
Product
EnVisio Patient Pad Transition Cushion, Model/Catalog Number: ENVISIO-SYS Product Description: The EnVisio Patient Pad Transition Cushion is a component of the EnVisio Navigation System which is a medical device that detects the presence of the SmartClip Soft Tissue Marker(s) an
Category
Medical Device
Distribution
17 states
HighNHTSA·24V607000·2025-01-08
Motorhome Overhead Cabinet Fasteners May Break and Cause Detachment
Motorhomes with HappiJac drop-down beds have front overhead cabinet fasteners that can break and detach while in motion. This can distract drivers and increase crash risk.
Product
HOLIDAY RAMBLER — 2022 HOLIDAY RAMBLER ADMIRAL
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V283000·2025-01-05
2025 Keystone Kodiak Travel Trailers Recalled for Defective Patio Support Struts
Keystone is recalling certain 2025 Kodiak travel trailers because the patio support struts may not adequately support the fold-down patio's weight, increasing the risk of injury. Owners should contact Keystone or their dealer for free repair.
Product
KEYSTONE — 2025 KEYSTONE KODIAK
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0762-2025·2025-01-01
MISHA Knee System Implants recalled due to fracture risk
Moximed is recalling 115 MISHA Knee System Implants in multiple US states due to a supplier component defect that may cause the implant to fracture, potentially leading to pain, swelling, and stiffness.
Product
MISHA Knee System Implant Small, Left, REF: 2-1001. MISHA Knee System Implant Small, Right, REF: 2-1002.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0654-2025·2024-12-25
Kirwan Surgical Disposable Bipolar Pencils recalled for potential tube failure
Kirwan Surgical Products is recalling 80,060 Disposable Bipolar Pencils (Model 14-5011) because the outer stainless-steel tube may break or detach during surgical use. The devices were distributed worldwide.
Product
Kirwan Surgical Products LLC Disposable 25-gauge bipolar pencil, straight. Model/Catalog Number: 14-5011 The Disposable Microsurgical Bipolar Pencil are designed for use in eye surgery, and other soft tissue procedures. For instance, the pencils are designed for cauterization
Category
Medical Device
Distribution
Distributed nationwide