The Recall Desk

Hazard

Structural Defect recalls

2,094 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,094
Critical
3
Severe
1,081
Most recent
2026-09-02

Of the 2,094 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 1,081 (52%) 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.

1626–1650 of 2094

  • HighFDA (Devices)·Z-2697-2014·2014-10-01

    Argon UltraStream Hemodialysis Catheter Recall Due to Luer Cracking

    Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because the red arterial luer may crack during attachment or manipulation.

    Product
    UltraStream Exchange Kit Model Numbers 32001524 (24 cm), 32001528 (28cm), 32001532 (32 cm), and 32001536 (36 cm) and 32002540 (40 cm). The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low arterial pr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2696-2014·2014-10-01

    Argon UltraStream Hemodialysis Catheters Recalled for Luer Cracking Risk

    Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because cracks may develop on the red arterial luer during use.

    Product
    UltraStream Chronic Hemodialysis Catheter Standard Kit; Model Number 32101524 (24 cm), 32101528 (28cm), 32101532 (32 cm), and 32101536 (36 cm) and 32102540 (40 cm). The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2698-2014·2014-10-01

    Argon UltraStream Hemodialysis Catheter Recalled for Luer Cracking

    Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because cracks may develop on the red arterial luer during attachment or manipulation.

    Product
    UltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 cm), and 32401536 (36 cm) and 32402540 (40 cm) The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low arterial
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V582000·2014-09-22

    Nissan Recalls 2014 Infiniti Hybrid Vehicles for Transmission Housing Defect

    Nissan is recalling 817 model year 2014 Infiniti Q50 and Q70 hybrid vehicles because damaged transmission housings could crack, creating road debris and disabling the vehicle.

    Product
    INFINITI — INFINITI Q50 HYBRID, Q70 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V574000·2014-09-19

    Navistar Recalls 2011-2012 Workhorse W62 Chassis for Exhaust Weld Defect

    Navistar is recalling 2011-2012 Workhorse W62 commercial chassis because a weld on the exhaust system may fatigue, allowing hot gases to enter the engine compartment and increasing fire risk.

    Product
    WORKHORSE — WORKHORSE W62
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2626-2014·2014-09-17

    Stryker Recalls Aria Implant Inserters Due to Product Fracturing Complaints

    Stryker Spine is recalling 64 units of Aria Standard and Specialty Implant Inserters due to complaints of product fracturing. The devices are used for spinal fusion procedures.

    Product
    Stryker Aria Implant Inserter, REF 48758500, This instrument is part of the Aria product brand. It is used for Implant insertion into the disc space. The Aria Inserter PEEK Spacer System offers implants that are interbody fusion devices intended for use as an aid in spinal f
    Category
    Medical Device
    Distribution
    24 states
  • HighFDA (Devices)·Z-2615-2014·2014-09-17

    Baxter Recalls Buretrol Solution Sets Due to Chamber Separation

    Baxter Healthcare is voluntarily recalling specific lots of Buretrol Solution Sets because the burette chamber may separate from the drip chamber.

    Product
    ***Baxter***Non-DEHP***BURETROL Solution Set 105" (2.7 m), 150 mL Burette***Drip Chamber Filter Valve 3 Luer Activated Valves***Male Luer Lock Adapter***with Retractable Collar***Fluid path is Sterile, Nonpyrogenic.***Indications for Use: For the administration of fluids from a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2596-2014·2014-09-17

    Primus Medical Recalls Transcend and Bariatric Mattresses Due to Delamination

    Primus Medical LLC is recalling specific Transcend and Bariatric mattresses because the top cover is delaminating. The recall affects 1,557 units distributed in the US and Canada.

    Product
    Prime Care ¿ Transcend Mattress, Prime Care ¿ Transcend Perimeter Mattress, Prime Care ¿ Transcend Advanced Mattress, Prime Care ¿ Transcend Advanced Perimeter Mattress, Prime Plus ¿ Bariatric Mattress and Prime Plus ¿ Bariatric Perimeter Mattress, individual units packaged seper
    Category
    Medical Device
    Distribution
    18 states
  • HighNHTSA·14V561000·2014-09-12

    Jayco Recalls 2015 Jay Flight Trailers Due to Ladder Mounting Defect

    Jayco is recalling 2015 Jay Flight 19RD trailers because the roof ladder may be installed on the wrong side without proper support, increasing injury risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2560-2014·2014-09-10

    OrthoPediatrics ACL Sleeve Installation Tool Recalled for Weld Fractures

    OrthoPediatrics Corp is recalling 56 ACL Sleeve Installation Tools due to weld fractures. The tools are used in pediatric and small stature adult ACL reconstruction systems.

    Product
    ACL Sleeve Installation Tool Sizes: 6mm, 6.5mm, 7.0mm, 7.5mm, 8.0mm, 8.5mm, 9.0mm, 10.0mm Product Usage: The OrthoPediatrics ACL Reconstruction System is a pediatric and small stature adult ACL reconstruction system that offers both the fixation devices and instrument in one
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V523000·2014-09-03

    Collins and Mid Bus School Buses Recalled for Body Joint Adhesive Defect

    NHTSA is recalling 281 model year 2014 Collins and Mid Bus school buses because inadequate adhesive on interior side panel joints may fail to meet federal safety standards.

    Product
    COLLINS — COLLINS, MID BUS DE416WR, DH416, SL408, DE516WR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2545-2014·2014-09-03

    Zimmer Patello-Femoral Knee Prosthesis Recalled for Forging Defects

    Zimmer, Inc. is recalling 15 units of a specific knee prosthesis component because internal review found five raw material forgings with defects that were not segregated.

    Product
    Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral Trochlea Component, Precoat, Size 4, Left. Knee prosthesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2245-2014·2014-08-27

    Zimmer Recalls Magna-Fx Cannulated Bone Screws Due to Leak Test Failure

    Zimmer, Inc. is recalling 47,682 units of Magna-Fx Cannulated Bone Screws because they failed a leak test due to damage of the inner cavity.

    Product
    Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw Sterile zimmer
    Category
    Medical Device
    Distribution
    45 states
  • SevereFDA (Devices)·Z-2177-2014·2014-08-20

    Carestream Recalls Kodak DirectView DR 7500 X-Ray Systems Due to Loose Parts

    Carestream Health is recalling 589 Kodak DirectView DR 7500 diagnostic x-ray systems because the x-ray tube assembly may detach from the overhead crane due to insufficiently tightened hardware.

    Product
    Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The DR 7500 system is a permanently installed diagnostic x-ray system composed of 4 main components: an operator console, over head tube crane, x-ray tube assembly including a collimator and stationary generator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2204-2014·2014-08-20

    Gambro Recalls Prismaflex HF 1000 Dialysis Sets Due to Connector Breakage

    Gambro Renal Products is recalling Prismaflex HF 1000 dialysis sets because connector breakages can cause leakage of liquid or blood.

    Product
    Prismaflex HF 1000. Product number 107140. Each set is packaged in a plastic pouch, 4 pouches per carton box
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2194-2014·2014-08-20

    Gambro Recalls Prisma TPE 2000 Sets Due to Connector Breakage

    Gambro Renal Products is recalling Prisma TPE 2000 sets because connector breakages can cause liquid or blood leakage.

    Product
    Prisma TPE 2000 set. Product number 109672. Each set is packaged in a plastic pouch, 4 pouches per carton box
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·14V489000·2014-08-08

    GM Recalls 2014-2015 Chevrolet Impala for Storage Console Latch Defect

    General Motors is recalling 2014-2015 Chevrolet Impala vehicles because the center storage console may not stay latched during a crash, increasing injury risk.

    Product
    CHEVROLET — CHEVROLET IMPALA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V483000·2014-08-06

    Ford Recalls 2015 Transit Vans for Sliding Door Defect

    Ford is recalling 2015 Transit cargo vans because windowless sliding doors may lack epoxy reinforcement, increasing the risk of occupant ejection in a side impact crash.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V446000·2014-07-23

    GM Recalls 2013-2015 Vehicles Due to Incomplete Seat Weld

    General Motors is recalling specific 2013-2015 Buick, Cadillac, Chevrolet, and GMC vehicles because an incomplete weld may cause front seats to detach during a crash.

    Product
    CADILLAC — CADILLAC, BUICK, CHEVROLET ATS, ENCORE, SILVERADO, CTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2053-2014·2014-07-23

    Stryker SHAPE Arm Dual SH2 Recalled for Potential Monitor Detachment

    Stryker Communications is recalling SHAPE Arm Dual SH2 brackets because the monitor mount may detach if specific hardware is missing.

    Product
    SHAPE ARM, DUAL SH2, an articulating, arm bracket that is attached to the service head of boom systems which are used for supporting and positioning equipment in operating rooms and patient care areas. The product comes as a component of kit part number 0682400254 and the Arm par
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2054-2014·2014-07-23

    Stryker Communications Recalls SHAPE Arm Monitor Mounts

    Stryker Communications is recalling SHAPE Arm monitor mounts because the mount may detach if a lock washer and screw are missing.

    Product
    SHAPE ARM, SINGLE WITH GCX MOUNT, an articulating, arm bracket that is attached to the service head of boom systems which are used for supporting and positioning equipment in operating rooms and patient care areas. The product comes as component of kit part number 0682400256 and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2055-2014·2014-07-23

    Stryker Communications Recalls SHAPE Arm Brackets for Boom Systems

    Stryker Communications is recalling 953 SHAPE Arm brackets used in operating rooms because the monitor mount may detach if specific hardware is missing.

    Product
    BAM (SHAPE) ARM, LEFT, an articulating, arm bracket that is attached to the service head of boom systems which are used for supporting and positioning equipment in operating rooms and patient care areas. The product comes as component of kit part number 0682000976, and the Arm p
    Category
    Medical Device
    Distribution
    Distributed nationwide