FDAJuly 14, 2026
Hollister Onli Catheters Recall Issued for Manufacturing Defect
FDA published this notice on July 14, 2026 for United States.
This notice is kept at its address for anyone who saved the link. AreaZine no longer holds the agency's full record for it, so the page shows what AreaZine recorded and links to the agency's own page, the one to read.
What AreaZine recorded
- Agency
- FDA
- Place
- United States
- Date
- July 14, 2026
- Recall class
- Class II
- Reason given by the agency
- Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might lead to genitourinary trauma or bleeding.
- Distribution
- US Nationwide distribution.
- Official source
- the notice at its source
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Source: FDA.