BullDogRecalls & reported problems across all models

We found 2 models of BullDog by Diversatek Healthcare, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

2 FDA recall records name at least one of these models by its device identifier.

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

BullDog 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. Nov 3, 2020Terminated

   Suction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure

   Z-0647-2021 · Root cause: Process control · Recall details · FDA record ↗

2. Nov 3, 2020Terminated

   Suction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure

   Z-0646-2021 · Root cause: Process control · Recall details · FDA record ↗

BullDog models

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

• BullDog® 1203-71

  Endoscopic Irrigation/Suction System
  1 recall0 reports
• BullDog 1203-72

  Endoscope Channel Accessory
  1 recall0 reports

Other Diversatek Healthcare, Inc. products

• Viper4 models · 0 reports · 4 recalls
• Zvu3 models · 1 reports · 2 recalls