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Medivators HookupRecalls & reported problems across all models

Medivators Inc. · 99 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

5 open recalls name at least one Medivators Hookup model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls
5

We found 99 models of Medivators Hookup by Medivators Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Mar 7, 2024 and Mar 7, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Difficult to Setup or Prepare” (1 report).

5 FDA recall records name at least one of these models by its device identifier, 5 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Reports received per month, all models

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 1 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Medivators Hookup recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. Jun 13, 2024Open, Classified

    IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly disinfected, which may present a risk of patient contamination or infection

    Z-2539-2024 · Root cause: Error in labeling · Recall details · FDA record ↗

  2. Jun 13, 2024Open, Classified

    IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly disinfected, which may present a risk of patient contamination or infection

    Z-2538-2024 · Root cause: Error in labeling · Recall details · FDA record ↗

  3. Jun 13, 2024Open, Classified

    IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly disinfected, which may present a risk of patient contamination or infection

    Z-2537-2024 · Root cause: Error in labeling · Recall details · FDA record ↗

  4. Jun 13, 2024Open, Classified

    IFU for hookup were incorrectly reflected within hookup IFUs and online reference system, Hookup Lookup (HULU). Use of an incorrect hookup connection and/or parameter set may prevent an endoscope from being properly disinfected, which may present a risk of patient contamination or infection

    Z-2536-2024 · Root cause: Error in labeling · Recall details · FDA record ↗

  5. Nov 13, 2023Open, Classified

    Identification label on affected hookups could become illegible over time due to the label's ink coming off. This may potentially prevent users from being able to effectively identify the hookup and may ultimately result in postponement of patient procedures.

    Z-0617-2024 · Root cause: Process control · names 96 of these models · Recall details · FDA record ↗

Most reported Medivators Hookup problems

Device problems

  • Device Difficult to Setup or Prepare1
  • Insufficient Device Problem Information1

Patient problems

  • Insufficient Information1
  • No Clinical Signs, Symptoms or Conditions1

Medivators Hookup models

99 models, most reported first. Each model has its own page with its reports, recalls and device details.

Recent Medivators Hookup adverse event reports

The 1 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Medivators Inc. products

All Medivators Inc. devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page