The Recall Desk

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.

26–50 of 293

  • HighFDA (Devices)·Z-1510-2026·2026-03-18

    Surgical Instrument Kit Recalled for Missing Cross-Pin in Impactor Handle

    Exactech is recalling the Equinoxe Core Instrument Kit because the impactor handle may be missing a cross-pin, potentially affecting surgical instrument functionality and safety. Approximately 596 kits were distributed across the United States and internationally.

    Product
    Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311X
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-1509-2026·2026-03-18

    Exactech Equinoxe Ergo Impactor Handles Recalled for Missing Cross-Pin

    Exactech is recalling 120 units of Equinoxe Ergo Modular Impactor Handles (Model 321-09-05) because the handle may be missing a cross-pin, a structural component that could compromise surgical function.

    Product
    Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-1512-2026·2026-03-18

    Waldemar Link Endo-Model Replacement Plateau Implant Bushing Detachment Risk

    Waldemar Link is recalling Endo-Model Replacement Plateau implants due to risk that the bushing could detach from the screw shaft due to longitudinal fracture.

    Product
    Endo-Model Replacement Plateau; Item Number: 15-0027/15;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·26308·2026-02-26

    Evajoy Above-Ground Pools Recalled for Drowning Risk from Compression Strap

    Evajoy above-ground pools 48 inches and taller are recalled due to a compression strap that creates a foothold, allowing children to access the pool and posing a drowning risk. No injuries have been reported.

    Product
    Evajoy 48-inch and taller above-ground pools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1311-2026·2026-02-11

    Molift Sling Bars Recalled for Structural Defect in Patient Lift Devices

    Molift 4-point sling bars are being recalled due to a bolt defect caused by material deformation between the lifting bar and device arm, which prevents proper device functionality.

    Product
    Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory to mobile hoists) Model/Catalog Number: 1430116,1430117,1430115 Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due to
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1309-2026·2026-02-11

    Molift Mover 300 mobile hoist recalled for bolt deformation defect

    ETAC A/S recalls Molift Mover 300 mobile hoists due to bolt deformation in the lifting bar joint that can prevent proper device functionality.

    Product
    Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: (1) M1501, (2) M1502, (3) M1504, (4) M15050, (5) M15151, (6) M15001, (7) M15002; Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1190-2026·2026-02-04

    Medline procedure convenience kits recalled for cracking tubing defect

    Medline medical procedure kits are being recalled due to complaints that butyrate tubing cracks during actuation of MASTISOL Liquid Adhesive vials. The kits are distributed nationwide.

    Product
    Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS, Kit SKU CDS984347O; 2) HEAD AND NECK CDS-LF, Kit SKU CDS984857N; 3) NECK PACK-LF, Kit SKU DYNJ0966130K; 4) NECKLINE PACK-LF, Kit SKU DYNJ51440B; 5) THYROID PACK, Kit SKU DYNJ58742J; 6) ENT I, K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1197-2026·2026-02-04

    Medline surgical procedure kits recalled for defective adhesive vial tubing

    Medline is recalling 1,928 medical procedure convenience kits due to defective tubing in MASTISOL liquid adhesive vials that may crack during use. The kits were distributed nationwide to healthcare facilities.

    Product
    Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY PACK-LF, Kit SKU DYNJ0395022O; 2) PELVISCOPY PACK-LF, Kit SKU DYNJ0415776Q; 3) DIVA PACK, Kit SKU DYNJ04811O; 4) DA VINCI PROSTATE/COLPOPEXY, Kit SKU DYNJ44864S; 5) MH ROBOTICS PACK, Kit SKU D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1186-2026·2026-02-04

    Medline Nerve Block Tray kits recalled for cracking tubing defect

    Medline Industries is recalling NERVE BLOCK TRAY 2 kits (SKU DYNJRA2713) due to complaints that butyrate tubing cracks during use of MASTISOL Liquid Adhesive. Affected kits should not be used.

    Product
    Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2, Kit SKU DYNJRA2713
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1193-2026·2026-02-04

    Medline Medical Procedure Convenience Kits Recalled for Cracking Tubing Defect

    Medline medical procedure convenience kits containing MASTISOL liquid adhesive are recalled due to reports that the butyrate tubing in the adhesive vials cracks during use. Approximately 857 units were distributed nationwide.

    Product
    Medline medical procedure convenience kits labeled as: 1) DRAWER 1 AIRWAY, Kit SKU ACC010270A; 2) DRAWER 2, Kit SKU ACC010690; 3) DRAWER 3 SYR/DRS/MON/NG 1 OF 3, Kit SKU ACC011073; 4) HYPOSPADIUS PACK, Kit SKU DYNJ00282Q; 5) SJ NEURO PACK RFID-LF, Kit SKU DYNJ0101360K;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V092000·2026-02-02

    2023 Tesla Model 3 and Model Y Power Steering Software Defect

    Tesla is recalling 376,241 2023 Model 3 and Model Y vehicles for a power steering defect that may cause loss of steering assist at low speeds, increasing crash risk.

    Product
    TESLA — 2023 TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26209·2026-01-22

    Cumbor Retractable Safety Gates Recalled for Child Entrapment Risk

    Aborder Products recalls Cumbor retractable safety gates due to a gap between the gate and floor that allows a child's torso to fit through, posing a risk of serious injury or death from entrapment. No injuries have been reported.

    Product
    Cumbor Retractable Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1044-2026·2026-01-21

    Nuclear Medicine System Detector Mounting Structural Defect Recall

    GE HealthCare recalls nuclear medicine systems that may have structural damage to detector mounting mechanisms due to improper transport. Damaged detectors could fall and cause serious injury, though no incidents have been reported.

    Product
    SMV DSX New Line, System, Tomography, Computed, Emission
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1101-2026·2026-01-21

    Portex Spinal Tray syringes recalled due to syringe collar cracks

    ICU Medical is recalling Portex Spinal Tray syringes due to cracks in the syringe collar. The defect may cause delayed blood draws, fluid leakage during arterial blood sampling, or improper delivery.

    Product
    Portex Spinal Tray, Item No. A3729-24 A3595
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V711000·2026-01-09

    2025 MINI Countryman S ALL4 front structure bolts may be improperly tightened

    BMW is recalling certain 2025 MINI Countryman S ALL4 vehicles because the bolts connecting the front body structure to the chassis may not be properly tightened. This could reduce crash protection for occupants.

    Product
    MINI — 2025 MINI COUNTRYMAN S ALL4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26181·2026-01-08

    Joyful Journeys baby loungers recalled for fall and entrapment hazards

    Approximately 9,300 Joyful Journeys baby loungers are recalled for violating infant sleep safety standards. The loungers have sides too low to contain infants and openings too wide, posing fall and entrapment hazards.

    Product
    Joyful Journeys Baby Loungers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0967-2026·2025-12-31

    Zimmer Affixus Femoral Nails Recalled for Potential Fatigue Fracture Risk

    Zimmer, Inc. is recalling 22 Affixus Antegrade Femoral Nailing systems due to an undersized distal diameter defect that could cause implant fatigue fracture. Potential complications include tissue damage and surgical intervention may be required.

    Product
    Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815509320 Software Version: N/A Product Description: Affixus 9 mm, Length 320 mm, Right, Trochanteric Nail Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0969-2026·2025-12-31

    Affixus Antegrade Femoral Nailing System Recalled for Implant Fracture Risk

    Zimmer is recalling specific lots of Affixus Antegrade Femoral Nails due to undersized distal diameter that could cause implant fracture. Affected patients may experience tissue damage or adverse reactions requiring additional surgery.

    Product
    Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815509360 Software Version: N/A Product Description: Affixus 9 mm, Length 360 mm, Right, Trochanteric Nail Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0974-2026·2025-12-31

    Affixus Antegrade Femoral Nails Recalled for Potential Implant Fracture

    Zimmer is recalling 11 Affixus Antegrade Femoral Nails due to potential undersized distal diameters that may cause implant fatigue fracture. Complications can include adverse tissue reaction, pain, non-union, or tissue damage requiring surgery.

    Product
    Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815609300 Software Version: N/A Product Description: Affixus 9 mm, Length 300 mm, Left, Trochanteric Nail Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0982-2026·2025-12-31

    Affixus Antegrade Femoral Nails Recalled for Undersized Distal Diameter

    Zimmer is recalling limited units of Affixus Antegrade Femoral Nails due to undersized distal diameter that may cause implant fracture. Potential complications include non-union, malunion, and tissue damage requiring surgical intervention.

    Product
    Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815809280 Software Version: N/A Product Description: Affixus 9 mm, Length 280 mm, Left, Priformis Nail Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·26162·2025-12-18

    SereneLife Above-Ground Pools 48 Inches and Taller Recalled for Drowning Hazard

    SereneLife Home is recalling about 80 above-ground pools 48 inches and taller because a compression strap creates unintended footholds that allow children to access and drown in the pool.

    Product
    SereneLife brand 48-inch and taller above-ground pools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0592-2026·2025-12-17

    FDA Recalls Draeger ErgoStar CM 55 Airway Connectors for Cracking

    Draeger's ErgoStar CM 55 airway connectors are being recalled due to cracks forming in the catheter mount hose. The defect affects respiratory connectivity in mechanical ventilation systems used for critically ill patients.

    Product
    ErgoStar CM 55, Model/Catalog Number: MP01855, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mechanically ventilated patient.
    Category
    Medical Device
    Distribution
    10 states
  • HighNHTSA·25V603000·2025-12-09

    Commercial trucks recalled for defective steering tie rod assembly

    Daimler Trucks is recalling commercial trucks and buses with defective tie rod assemblies that may cause loss of steering control. Dealers will inspect and replace them free of charge.

    Product
    FREIGHTLINER — 2024 FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0531-2026·2025-12-03

    SJM Pericardial Patch Recalled for Tensile Strength Deficiency

    Glycar SA recalls SJM Pericardial Patches (Model C0914) that may not meet required tensile strength specifications. 30 units were distributed in the US.

    Product
    SJM Pericardial Patch, with EnCap Technology 9x14cm, Model Number REF C0914; PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0488-2026·2025-11-26

    FDA Recalls TMJ Bilateral Implants Due to Screw Hole Position Discrepancy

    TMJ Solutions Inc is recalling 63 TMJ bilateral implants (model CHG020) due to a discrepancy in screw hole positioning. The affected implants were distributed to patients in multiple U.S. states and internationally to Canada, Spain, and Brazil.

    Product
    TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    15 states