FDAJuly 29, 2026
Windstone AMS Convenience Kit Recall Over Detached Break-off-Parts in Sodium Chloride Bags
FDA published this notice on July 29, 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 29, 2026
- Recall class
- Class II
- Reason given by the agency
- The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the infusion port during manipulation.
- Distribution
- US Nationwide distribution in the states of CA, GA, WA.
- Official source
- the notice at its source
Official warnings by state, with every type counted since 2008Search notices, places and declaration numbers
Source: FDA.