The Recall Desk

Hazard

Lodged Accessories 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
2016-07-06

Of the 4 lodged accessories 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 lodged accessories 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

  • HighFDA (Devices)·Z-2068-2016·2016-07-06

    Pentax Medical Recalls Colonoscopes Due to Lodged Accessories

    Pentax Medical is recalling 12,412 colonoscopes because operational and cleaning accessories can become lodged in the instrument channel.

    Product
    Colonoscope Intended to provide optical visualization of and therapeutic access to the Lower Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Large Bowel to the Cecum. The instrument is introduced via the rectum when in
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2080-2016·2016-07-06

    Pentax Small Bowel Scope Recall Due to Lodged Accessories

    Pentax Medical Company is recalling 96 Small Bowel Scopes because operational and cleaning accessories can become lodged in the instrument channel.

    Product
    Small Bowel Scope Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Esophagus, Stomach and Duodenum. The instrument is introduced via the mouth when indications consistent with the need for procedure are observed in adul
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2077-2016·2016-07-06

    Pentax Ultrasound Gastroscope Recall Due to Lodged Accessories

    Pentax Medical Company is recalling ultrasound gastroscopes because operational and therapeutic accessories can become lodged in the instrument channel.

    Product
    Ultrasound Gastroscope Intended to provide optical visualization of, ultrasonic visualization of and therapeutic access to, the Upper Gastrointestinal Track including but not restricted to organs, tissues and subsystems: Esophagus, Stomach, Duodenum, Small Bowel and underlying a
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2079-2016·2016-07-06

    Pentax Medical Recalls Esophagoscopes Due to Lodged Accessories Risk

    Pentax Medical is recalling 405 esophagoscopes because operational accessories can become lodged in the instrument channel.

    Product
    Esophagoscope Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Esophagus, Stomach and Duodenum. The instrument is introduced via the mouth when indications consistent with the need for procedure are observed in adult an
    Category
    Medical Device
    Distribution
    2 states