The Recall Desk

Hazard

Structural Defect recalls

2,112 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,112
Critical
3
Severe
1,155
Most recent
2026-10-20

Of the 2,112 structural defect recalls we have scored against our rubric, 3 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,155 (55%) 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 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.

601–625 of 2112

  • SevereFDA (Devices)·Z-1476-2021·2021-04-28

    Smiths Medical Recalls Manifold Rotators Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific lots of manifold rotators and related components because they may have insufficient or incomplete welds.

    Product
    Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR, OFF HANDLE, Model Number MX1232MR b. 250 3 GANG MANIFOLD ROTATOR, OFF HANDLE, Model Number MX1233MR c. 550 2 GANG MANIFOLD ROTATOR, OPEN HANDLE, Model Number MX1322MR d. 550 3 GANG MANIFOLD ROTATOR, OFF HANDLE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1479-2021·2021-04-28

    Smiths Medical Recalls High Pressure Rotators Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific lots of Medex High Pressure Rotators because they may have insufficient or incomplete welds.

    Product
    HIGH PRESSURE ROTATOR (Component) a. WITH MALE LUER LOCK, Model Number MX496HP b. WITH FEMALE LUER LOCK, Model Number MX497HP. component of extravascular blood-pressure Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1481-2021·2021-04-28

    Smiths Medical Recalls Medex Pressure Injector Lines Due to Weld Defects

    Smiths Medical ASD Inc. is recalling specific lots of Medex pressure injector lines and related components due to insufficient or incomplete welds.

    Product
    Medex 10 IN Pressure Injector Line w/Rot (1200psi) NS. REF B1681R, component of extravascular blood-pressure Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1474-2021·2021-04-28

    Smiths Medical Recalls Medex High Pressure Adaptors and LogiCal Kits

    Smiths Medical ASD Inc. is recalling specific lots of Medex High Pressure Adaptors and LogiCal Kits due to insufficient or incomplete welds.

    Product
    Gang Cath Lab Set, Model Number M20858R1.for the administration of IV fluids. Stopcocks and manifolds are used to control the direction of IV fluid flow.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1477-2021·2021-04-28

    Smiths Medical Recalls Stopcock Rotators Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific stopcock rotator components used in cardiac kits due to insufficient or incomplete welds.

    Product
    Stopcock rotator (Component): a. 1050 STOPCOCK ROTATOR, OFF HANDLE, Model Number MX1431MR b. 1050 STOPCOCK LEFT ROTATOR, OFF HANDLE, Model Number MX1431MRL c. 700 PSI STPCK W/ ROTATOR, Model Number MX4331R. Stopcocks and manifolds used to control the direction of IV fluid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1475-2021·2021-04-28

    Smiths Medical Recalls Medex High Pressure Adaptors and LogiCal Kits

    Smiths Medical is recalling specific lots of Medex High Pressure Adaptors and LogiCal Kits due to potential manufacturing defects in welds.

    Product
    ANGIOGRAPHIC KIT W/MX123-3MR MANIFOLD, Model Number MX1030. for use during angiography and other special procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1480-2021·2021-04-28

    Smiths Medical Recalls Tubing Components Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific lots of tubing components for blood-pressure transducers due to insufficient or incomplete welds.

    Product
    Tubing with male luer lock adapter (Component) a. 76 cm, REF 601280 b. 122 cm, REF 607281. component of extravascular blood-pressure Transducer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1478-2021·2021-04-28

    Smiths Medical Recalls Medex High Pressure Tubing Due to Weld Defects

    Smiths Medical ASD Inc. is recalling specific lots of Medex high pressure tubing and components due to insufficient or incomplete welds.

    Product
    HIGH PRESSURE TUBING, 72IN, Model Number MX152114 (Component). Stopcocks and manifolds are used to control the direction of IV fluid flow.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1470-2021·2021-04-28

    Smiths Medical Recalls LogiCal Monitoring Sets Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific lots of LogiCal Monitoring Sets and related components due to insufficient or incomplete welds.

    Product
    LogiCal Monitoring Set, Model Number DPS564898. for blood pressure monitoring and blood sampling.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1472-2021·2021-04-28

    Smiths Medical Recalls Left Heart Kits Due to Incomplete Welds

    Smiths Medical ASD Inc. is recalling specific lots of Left Heart Kits and related components due to insufficient or incomplete welds.

    Product
    Left Heart Kit, Model Number M20268. for blood pressure monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V302000·2021-04-28

    2021 Hyundai Elantra seat back recliner frame welding defect

    Hyundai is recalling certain 2021 Elantra vehicles because the driver and front passenger seat back recliners may have been improperly welded and could separate during a crash, increasing injury risk.

    Product
    HYUNDAI — HYUNDAI ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V297000·2021-04-27

    Mitsubishi Fuso Recalls FEC7T Trucks for Rear Leaf Spring Defect

    Mitsubishi Fuso is recalling 2019-2021 FEC7T trucks because the rear leaf spring may break, creating a road hazard and increasing crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC7T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V263000·2021-04-15

    Subaru Recalls Crosstrek and Forester for Rear Stabilizer Bolt Defect

    Subaru is recalling 2018-2019 Crosstrek and 2019 Forester vehicles because rear stabilizer bracket bolts may loosen and detach, increasing crash risk.

    Product
    SUBARU — SUBARU CROSSTREK, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1343-2021·2021-04-14

    Fenwal Recalls Amicus MNC Apheresis Kits Due to Centrifuge Pack Leaks

    Fenwal Inc is recalling specific lots of Amicus MNC Apheresis Kits because centrifuge packs may leak blood during therapeutic procedures.

    Product
    Amicus MNC Apheresis Kit - Double Needle - Product Usage: intended for use in the collection of blood components and mononuclear cells.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1379-2021·2021-04-14

    Howmedica Recalls Specialty Triathlon TS Trial Cutting Guides Due to Fracture Risk

    Howmedica Osteonics Corp. is recalling Specialty Triathlon TS Trial Cutting Guides because the posterior condyle may fracture during transport or surgery.

    Product
    Trial Cutting Guide for Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee System, prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer. Catalog Number: I-K3834CG00 Specialty Triathlon TS Trial Cutting Guide Set…
    Category
    Medical Device
    Distribution
    7 states
  • SevereNHTSA·21V258000·2021-04-13

    2021 Newmar Motorhomes Recall: Steering Column Shaft Disengagement Risk

    Newmar is recalling certain 2021 motorhomes due to a steering output shaft that may be too short and disengage from the input shaft, potentially causing loss of steering control and increased crash risk. Owners should contact Newmar for free inspection and replacement.

    Product
    NEWMAR — NEWMAR NEW AIRE, DUTCH STAR, MOUNTAIN AIRE, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V248000·2021-04-08

    Jaguar Recalls XE Vehicles for Weak Rear Rail Assembly

    Jaguar is recalling 2017-2018 and 2020 XE vehicles because missing spot welds may weaken the rear rail assembly, increasing the risk of a crash during towing.

    Product
    JAGUAR — JAGUAR XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V243000·2021-04-07

    Utility Trailer Recalls VS2DC, VS2DX, VS3DX Models for Missing Weld

    Utility Trailer is recalling 2006-2021 VS2DC, VS2DX, and VS3DX trailers because a missing weld may cause the slider rail to detach, increasing crash risk.

    Product
    UTILITY TRAILER — UTILITY TRAILER VS3DX, VS2DX, VS2DC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V236000·2021-04-05

    2021 Forest River Flagstaff and Rockwood Fifth Wheels Pin Box Defect

    Forest River is recalling certain 2021 Flagstaff and Rockwood fifth wheels due to pin box defects. The pin box may be under-rated for the vehicle's gross weight rating, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V231000·2021-04-01

    2021 Mercedes-Benz GLB vehicles recalled for potentially detaching tailgate spoilers

    Mercedes-Benz is recalling certain 2021 GLB35 AMG and 2020–2021 GLB250 vehicles because the side spoilers on the tailgate might not have been installed correctly, allowing them to detach and create a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250, AMG GLB35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1294-2021·2021-03-31

    Teleflex Recalls Rusch Polaris Laryngoscopes Due to Handle Cracking

    Teleflex is voluntarily recalling Rusch Polaris laryngoscopes because customers reported that the handles develop cracks or break at the hinge.

    Product
    RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1257-2021·2021-03-24

    Cordis Precise Pro RX Carotid Stent Recall for Tip Separation

    Cordis is recalling Precise Pro RX Carotid Stent implant systems because the distal tip may separate from the lumen wire.

    Product
    PRECISE PRO RX CAROTID STENT implant system, Product Codes: PC0520RXC, PC0530RXC, PC0540RXC, PC0620RXC, PC0630RXC, PC0640RXC, PC0720RXC, PC0730RXC, PC0740RXC, PC0820RXC, PC0830RXC, PC0840RXC, PC0920RXC, PC0930RXC, PC0940RXC, PC1030RXC, PC1040RXC
    Category
    Medical Device
    Distribution
    2 states