ChemoPlusRecalls & reported problems across all models
Cardinal Health 200, LLC · 14 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one ChemoPlus model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 14 models of ChemoPlus by Cardinal Health 200, LLC 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
ChemoPlus 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.
- Nov 12, 2025Class IIOpen, Classified
Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.
Z-0897-2026 · Root cause: Under Investigation by firm · names 14 of these models · Recall details · FDA record ↗
ChemoPlus models
14 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ChemoPlus CT5502TSGOWN, SURGICAL1 recall0 reports
- ChemoPlus CT5503TSGOWN, SURGICAL1 recall0 reports
- ChemoPlus CT5504TSGOWN, SURGICAL1 recall0 reports
- ChemoPlus CT5505TSGOWN, SURGICAL1 recall0 reports
- ChemoPlus CT5500TACCESSORY, SURGICAL APPAREL1 recall0 reports
- ChemoPlus CT5500TSACCESSORY, SURGICAL APPAREL1 recall0 reports
- ChemoPlus CT5502TGOWN, SURGICAL1 recall0 reports
- ChemoPlus CT5503TGOWN, SURGICAL1 recall0 reports
- ChemoPlus CT5504TGOWN, SURGICAL1 recall0 reports
- ChemoPlus CT5505TGOWN, SURGICAL1 recall0 reports
- ChemoPlus DP5003GTGOWN, SURGICAL1 recall0 reports
- ChemoPlus DP5001GTGOWN, SURGICAL1 recall0 reports
- ChemoPlus DP5002GTGOWN, SURGICAL1 recall0 reports
- ChemoPlus DP5004GTGOWN, SURGICAL1 recall0 reports
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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