Good WorksRecalls & reported problems across all models

We found 4 models of Good Works by Bosma Enterprises in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device identifier, 1 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

Good Works 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. Aug 14, 2026Open, Classified

   Gloves may exhibit defects such as tears, missing fingers, and debris. Use of defective gloves may lead to healthcare personnel and patient exposure to infectious pathogens leading to infection or cross-contamination, or exposure to chemical agents leading to irritation or systemic toxicities.

   Z-3289-2026 · Root cause: Process control · names 4 of these models · Recall details · FDA record ↗

Good Works models

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

• Good Works 72-50604

  Polymer Patient Examination Glove
  1 recall0 reports
• Good Works 72-50603

  Polymer Patient Examination Glove
  1 recall0 reports
• Good Works 72-50601

  Polymer Patient Examination Glove
  1 recall0 reports
• Good Works 72-50602

  Polymer Patient Examination Glove
  1 recall0 reports