Endoscopic Cleaning Brushes sold in various Endoscopy Kits — Class II medical device recall Z-2203-2019
Terminated recall by Medline Industries Inc, reported 2019-08-14, distributed nationwide. Potential risk of brush detachment during cleaning. If brush detachment is not identified, there is the potent
| Recall number | Z-2203-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2019-04-25 |
| Classified | 2019-08-06 |
| Reported by FDA | 2019-08-14 |
| Terminated | 2020-12-16 |
| Distributed | Nationwide (US) |
| Quantity | 22,204 |
| Reason classes | device malfunction |
| Lot numbers | GJ25, GM10, HA05, HA20 |
Product
Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product Usage: The brushes are used to help clean out the endoscopes in between patient procedures.
Reason for recall
Potential risk of brush detachment during cleaning. If brush detachment is not identified, there is the potential for the brush to be left within the scope.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2203-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.