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CURADRecalls & reported problems across all models

Medline Industries, Inc. · 85 models in the FDA device registry

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

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

Adverse event reports
295
Deaths reported
0
Injuries reported
7
Recalls
4

We found 85 models of CURAD by Medline Industries, Inc. in the FDA's device registry (GUDID). Together they are named in 295 adverse event reports in the FDA's MAUDE database, received between Aug 10, 2017 and Sep 30, 2026 — classified as 7 injuries, 284 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (185 reports).

4 FDA recall records name at least one of these models by its device identifier, 4 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: 0 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: 1 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 1 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 2 reportsMay 2026: 5 reportsJun 2026: 3 reportsJul 2026: 0 reportsAug 2026: 9 reportsSep 2026: 269 reportsOct 2026: 0 reports202420252026269
Last 36 months. The most recent month may be incomplete.

CURAD 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. Oct 27, 2025Open, Classified

    Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.

    Z-0904-2026 · Root cause: Package design/selection · Recall details · FDA record ↗

  2. Oct 27, 2025Open, Classified

    Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.

    Z-0903-2026 · Root cause: Package design/selection · Recall details · FDA record ↗

  3. Oct 27, 2025Open, Classified

    Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.

    Z-0902-2026 · Root cause: Package design/selection · Recall details · FDA record ↗

  4. Oct 27, 2025Open, Classified

    Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.

    Z-0901-2026 · Root cause: Package design/selection · Recall details · FDA record ↗

Most reported CURAD problems

Device problems

  • Loss of or Failure to Bond185
  • Adhesive Too Strong44
  • Product Quality Problem13
  • Material Split, Cut or Torn12
  • Biocompatibility10
  • Material Puncture/Hole5
  • Appropriate Device Problem Term/Code Not Available4
  • Material Frayed4

Patient problems

  • No Clinical Signs, Symptoms or Conditions222
  • Skin Tears24
  • Skin Inflammation/ Irritation15
  • Insufficient Information11
  • Pain9
  • Hemorrhage/Blood Loss/Bleeding8
  • Blister6
  • Erythema6

CURAD models

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

Recent CURAD adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Medline Industries, Inc. products

All Medline Industries, Inc. devices →

Sources and updates

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