The Recall Desk

Hazard

Mechanism Failure recalls

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

What the numbers show

Total
4
Critical
0
Severe
0
Most recent
2026-03-19

Of the 4 mechanism failure 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.

Which agencies issued them

About this hazard tag

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

1–4 of 4

  • HighCPSC·26334·2026-03-19

    Amazon Basics folding pocket knife may not stay secured closed

    Amazon is recalling the Amazon Basics Camping Folding Pocket Knife because the folding mechanism can fail to remain properly secured in the closed position, posing a laceration hazard.

    Product
    Amazon Basics Camping Folding Pocket Knives
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25444·2025-08-28

    Locking carabiners recalled because the automatic closing mechanism can break

    About 12,600 Nimbus Lock Carabiners are recalled because the automatic closing mechanism can break and prevent the gate from closing, posing a fall risk. There are 21 reports of breakage; no injuries reported.

    Product
    Nimbus Lock Carabiners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1811-2021·2021-06-16

    Alphatec Insignia Anterior Cervical Plate System screw locking mechanism failure

    Alphatec Spine is recalling the Insignia Anterior Cervical Plate System due to a potential failure in the screw locking mechanism. The mechanism may disassociate or unlock during or after spinal surgery.

    Product
    Atec Insignia Anterior Cervical Plate System, REF 136-0240 Insignia, ACP, 2-Level, 40 mm, Rx Only, Non-Sterile, UDI: (01)00190376268408
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1818-2021·2021-06-16

    Alphatec Insignia Anterior Cervical Plate: Screw Blocking Mechanism May Disassociate

    Alphatec Spine is recalling the Insignia Anterior Cervical Plate System because the screw blocking mechanism may disassociate during or after spinal surgery.

    Product
    Atec Insignia Anterior Cervical Plate System, REF 136-0354 Insignia, ACP, 3-Level, 54 mm, Rx Only, Non-Sterile, UDI: (01)00190376268583
    Category
    Medical Device
    Distribution
    Distributed nationwide