CurityRecalls & reported problems across all models
Cardinal Health 200, LLC · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one Curity 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
- 1
- Recalls
- 1
We found 2 models of Curity by Cardinal Health 200, LLC 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 26, 2025 and Mar 26, 2025 — classified as 1 injury.
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
Reports received per month, all models
Curity 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.
- Apr 17, 2024Class IIOpen, Classified
Potential contamination of the product with latex adhesive residual.
Z-1835-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported Curity problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Skin Inflammation/ Irritation1
Curity models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Curity 44102Tape and bandage, adhesive1 recall0 reports
- Curity 9190AGauze / sponge,nonresorbable for external use1 report
Recent Curity adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryMar 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE CUSTOMER REPORTED THAT OVER THE LAST 4-5 WEEKS, PATIENTS ARE GETTING REACTIONS SO BAD TO THE PRODUCT, IT LOOKS LIKE BURNS IN A PERFECT OUTLINE OF THE ABDOMINAL PAD SHAPE. THEY ARE HAVING TO TREAT PATIENTS WITH ANTIBIOTICS FOR IT. PER ADDITIONAL INFORMATION RECEIVED, IT WAS A BURN LIKE REACTION IN THE SHAPE OF THE ABDOMINAL PADS. THE PATIENTS WERE PRESCRIBED PREDNISONE. THE ONLY RELIEF THEY GOT WAS WHEN THE ABDOMINAL PADS WERE REMOVED. PHOTOS CANNOT PROVIDE PHOTOS DUE TO PATIENT PRIVACY.
Patient problems: Skin Inflammation/ Irritation
MAUDE report 21697320 ↗
Other Cardinal Health 200, LLC products
- JACKSON-PRATT20 models · 13 reports · 19 recalls
- Monoject35 models · 96 reports · 11 recalls
- CONVERTORS38 models · 40 reports · 11 recalls
- Argyle33 models · 58 reports · 7 recalls
- Salem Sump31 models · 40 reports · 7 recalls
- Dover45 models · 241 reports · 2 recalls
- Kendall31 models · 51 reports · 3 recalls
- Kangaroo35 models · 130 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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