HALF APRONRecalls & reported problems across all models
Burlington Medical, LLC · 26 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one HALF APRON 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 26 models of HALF APRON by Burlington Medical, 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
HALF APRON 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.
- Feb 11, 2026Open, Classified
Potential for attenuation degradation over time, decreasing the lifespan.
Z-1762-2026 · Root cause: Process change control · names 26 of these models · Recall details · FDA record ↗
HALF APRON models
26 models, most reported first. Each model has its own page with its reports, recalls and device details.
- HALF APRON R8HALF1HApron, Protective1 recall0 reports
- HALF APRON R8HALF3HApron, Protective1 recall0 reports
- HALF APRON R8HALF4HApron, Protective1 recall0 reports
- HALF APRON R8HALF5HApron, Protective1 recall0 reports
- HALF APRON R8HALF6HApron, Protective1 recall0 reports
- HALF APRON R8HALF1BApron, Protective1 recall0 reports
- HALF APRON R8HALF2BApron, Protective1 recall0 reports
- HALF APRON R8HALF3BApron, Protective1 recall0 reports
- HALF APRON R8HALFS8TBApron, Protective1 recall0 reports
- HALF APRON R8HALF4BApron, Protective1 recall0 reports
- HALF APRON R8HALF5BApron, Protective1 recall0 reports
- HALF APRON R8HALF6BApron, Protective1 recall0 reports
- HALF APRON S8HALF3HApron, Protective1 recall0 reports
- HALF APRON S8HALF4HApron, Protective1 recall0 reports
- HALF APRON S8HALF5HApron, Protective1 recall0 reports
- HALF APRON S8HALF6HApron, Protective1 recall0 reports
- HALF APRON S8HALF1BApron, Protective1 recall0 reports
- HALF APRON S8HALF2BApron, Protective1 recall0 reports
- HALF APRON S8HALF3BApron, Protective1 recall0 reports
- HALF APRON S8HALFS8TBApron, Protective1 recall0 reports
- HALF APRON S8HALF4BApron, Protective1 recall0 reports
- HALF APRON S8HALF6BApron, Protective1 recall0 reports
- HALF APRON U8HALF6HApron, Protective1 recall0 reports
- HALF APRON U8HALF1BApron, Protective1 recall0 reports
- HALF APRON U8HALF3BApron, Protective1 recall0 reports
- HALF APRON U8HALF4BApron, Protective1 recall0 reports
Other Burlington Medical, LLC products
- CAP8 models · 2 reports · 1 recall
- Thyroid Shield BAT3 models · 0 reports · 1 recall
- VEST48 models · 0 reports · 1 recall
- KILT BLOCKER12 models · 0 reports · 1 recall
- DHALF5 models · 0 reports · 1 recall
- LEG WRAP10 models · 0 reports · 1 recall
- KILT50 models · 0 reports · 1 recall
- SLEEVE15 models · 0 reports · 1 recall
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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