Lucky Super SoftRecalls & reported problems across all models

We found 2 models of Lucky Super Soft by Delta Brands Inc. 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

Lucky Super Soft 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. Dec 26, 2025Open, Classified

   Potential exposure of rodents and rodent activity in the distribution center.

   Z-1180-2026 · Root cause: Storage · names 2 of these models · Recall details · FDA record ↗

Lucky Super Soft models

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

• Lucky Super Soft Bandages in differenet size

  Tape And Bandage, Adhesive
  1 recall0 reports
• Lucky Super Soft Kit

  First Aid Kit Without Drug
  1 recall0 reports