The Recall Desk

Hazard

Incorrect Dimension recalls

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

What the numbers show

Total
7
Critical
0
Severe
0
Most recent
2020-10-07

Of the 7 incorrect dimension recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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 incorrect dimension 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.

1–7 of 7

  • HighFDA (Devices)·Z-3019-2020·2020-10-07

    Exactech Recalls Equinoxe Reverse Shoulder Compression Screw Kits

    Exactech is recalling Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kits because they may contain screws of incorrect length.

    Product
    Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm.
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-3020-2020·2020-10-07

    Exactech Recalls Equinoxe Reverse Shoulder Compression Screw Kits

    Exactech is recalling Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kits because they may contain screws of incorrect length.

    Product
    Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm.
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0753-2020·2020-01-08

    Medicrea Polyaxial Pedicle Screws Recalled Due to Incorrect Length

    Medicrea International is recalling 210 polyaxial pedicle screws that are 50mm long instead of the labeled 45mm, posing a risk of nerve contact and postoperative pain.

    Product
    Medicrea Pass LP, REF B02217545, Non Sterile, Material: Ti-6Al-4V ELI, VIS PEDICULAIRE POLYAXIALE 7.5MM x 45MM, POLYAXIAL PEDICLE SCREW 7.5MM x 45 MM, POLYAXIAL PEDIKELSCHRAUBE 7.5MM X 45MM, TORNILLO PEDICULAR POLIAXIAL 7.5MM x 45MM VITE POLIASSIALE PEDUNCOLARE 7.5MM x 45MM, PAR
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1105-2018·2018-03-28

    Smith & Nephew Legion HK Femoral Wedge Recall Due to Incorrect Screw Size

    Smith & Nephew is recalling Legion HK Femoral Wedge components because the included screws are 5 mm instead of 10 mm, making them too short for use.

    Product
    smith&nephew, LEGION HK FEMORAL WEDGE (WEDGE AND SCREW), 5 MM, SIZE 5, REF 71422159, QTY: (1), STERILE The Revision Knee System Components are indicated for rheumatoid arthritis; post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age,
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0316-2018·2018-01-10

    Amendia Recalls Ceres Self-Drilling Variable Screws Due to Incorrect Length Marking

    Amendia, Inc. is recalling 40 Ceres Self-Drilling Variable Screws because some units marked as 12 mm actually measure 14 mm in length.

    Product
    Ceres Self-Drilling Variable Screw 4.0 x 12mm The Ceres screws are self-drilling variable screws that are intended to be used with the Ceres-C Stand-Alone Cervical System.
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1029-2016·2016-03-09

    Argon Medical Devices Recalls ClosureFast Introducer Sheath Sets Due to Assembly Error

    Argon Medical Devices is recalling specific ClosureFast Introducer Sheath Sets because incorrect sheath lengths were assembled to the devices.

    Product
    ClosureFast Micro Introducer Sheath Set 7Fr/Ch(2.3mm) x 7 cm REF MIS-F707 and ClosureFast Introducer Sheath Set 7Fr/Ch(2.3mm) x 11 cm REF IS-7F11. Indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2151-2012·2012-08-15

    ConMed Linvatec Recalls PopLok Bone Punch Due to Incorrect Shaft Diameter

    ConMed Linvatec recalled one lot of PopLok bone punches because the metal shaft diameter was 4.5mm instead of the intended 3.5mm.

    Product
    PopLok Punch labeled in part: "PKL-35M***3.5mm***QTY 1***PopLok Punch***ConMed Linvatec Biomaterials, Ltd. Hermiankatu 6-8L 33720 Tampere, FINLAND***Rx Only***ConMed Linvatec 11311 Concept Blvd Largo, FL 33773-4908 USA***Made in USA***" Intended Use: Bone Punch.
    Category
    Medical Device
    Distribution
    0 states