Recall archive / FDA company announcement
Aligned Medical Angio Pack: Angio Packs (AMS6908E and AMS6908F) — FDA announcement Apr 20, 2026
Published notice; closure not supplied
A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.
Source date Apr 20, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Angio Packs (AMS6908E and AMS6908F)
- Reason
- Risk of the syringe rotating adapter unwinding during use, which may result in a loose connection and/or full disconnection between the syringes and manifold, potentially causing biohazard exposure, blood loss, infection, or air embolism.
- Classification
- Not supplied
- Recalling firm
- Windstone Medical Packaging dba Aligned Medical Solutions
- Quantity
- Not supplied
- Agency-reported status
- Company recall announcement
- Source record identifier
- 0c08ca2abd291424
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Brand | Aligned Medical Solutions; Kit Name | Product Code | DI Number | Lot; Angio Pack | AMS6908E | B098AMS6908E0 | 214875; Angio Pack | AMS6908F | B098AMS6908F0 | 215436, 225001, 226706, 234088 |
Match all identifying details in the current notice. A brand name alone is not enough.
Product tables from the announcement
These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.
| Brand | Aligned Medical Solutions | ||
| Kit Name | Product Code | DI Number | Lot |
| Angio Pack | AMS6908E | B098AMS6908E0 | 214875 |
| Angio Pack | AMS6908F | B098AMS6908F0 | 215436, 225001, 226706, 234088 |
Announcement retrieved Oct 1, 2026. Official announcement.
Distribution
Aligned Medical Solutions distributed these kits nationwide. Recalled Product(s) were manufactured from 10/18/2024 to 11/13/2025 and distributed from 10/28/24 to 11/28/2025
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Fda listing date
- Apr 20, 2026
- Company announcement date
- Apr 16, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.