--- title: "Aligned Medical Angio Pack: Angio Packs (AMS6908E and AMS6908F) — FDA announcement Apr 20, 2026 | Is It on Recall" description: "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, p" url: https://isitonrecall.com/recall/fdapress-0c08ca2abd291424-aligned-medical-angio-pack-angio-packs-ams6908e-and-ams6908f/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## 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 [Open the official record](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/windstone-medical-packaging-dba-aligned-medical-solutions-issues-nationwide-recall-namic) ## 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. **FDA company announcement, table 1** | Column 1 | Column 2 | Column 3 | Column 4 | | --- | --- | --- | --- | | Brand | Aligned Medical Solutions | Aligned Medical Solutions | 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](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/windstone-medical-packaging-dba-aligned-medical-solutions-issues-nationwide-recall-namic). ## 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](https://isitonrecall.com/state/alaska/) - [Alabama](https://isitonrecall.com/state/alabama/) - [Arkansas](https://isitonrecall.com/state/arkansas/) - [Arizona](https://isitonrecall.com/state/arizona/) - [California](https://isitonrecall.com/state/california/) - [Colorado](https://isitonrecall.com/state/colorado/) - [Connecticut](https://isitonrecall.com/state/connecticut/) - [Delaware](https://isitonrecall.com/state/delaware/) - [Florida](https://isitonrecall.com/state/florida/) - [Georgia](https://isitonrecall.com/state/georgia/) - [Hawaii](https://isitonrecall.com/state/hawaii/) - [Iowa](https://isitonrecall.com/state/iowa/) - [Idaho](https://isitonrecall.com/state/idaho/) - [Illinois](https://isitonrecall.com/state/illinois/) - [Indiana](https://isitonrecall.com/state/indiana/) - [Kansas](https://isitonrecall.com/state/kansas/) - [Kentucky](https://isitonrecall.com/state/kentucky/) - [Louisiana](https://isitonrecall.com/state/louisiana/) - [Massachusetts](https://isitonrecall.com/state/massachusetts/) - [Maryland](https://isitonrecall.com/state/maryland/) - [Maine](https://isitonrecall.com/state/maine/) - [Michigan](https://isitonrecall.com/state/michigan/) - [Minnesota](https://isitonrecall.com/state/minnesota/) - [Missouri](https://isitonrecall.com/state/missouri/) - [Mississippi](https://isitonrecall.com/state/mississippi/) - [Montana](https://isitonrecall.com/state/montana/) - [North Carolina](https://isitonrecall.com/state/north-carolina/) - [North Dakota](https://isitonrecall.com/state/north-dakota/) - [Nebraska](https://isitonrecall.com/state/nebraska/) - [New Hampshire](https://isitonrecall.com/state/new-hampshire/) - [New Jersey](https://isitonrecall.com/state/new-jersey/) - [New Mexico](https://isitonrecall.com/state/new-mexico/) - [Nevada](https://isitonrecall.com/state/nevada/) - [New York](https://isitonrecall.com/state/new-york/) - [Ohio](https://isitonrecall.com/state/ohio/) - [Oklahoma](https://isitonrecall.com/state/oklahoma/) - [Oregon](https://isitonrecall.com/state/oregon/) - [Pennsylvania](https://isitonrecall.com/state/pennsylvania/) - [Rhode Island](https://isitonrecall.com/state/rhode-island/) - [South Carolina](https://isitonrecall.com/state/south-carolina/) - [South Dakota](https://isitonrecall.com/state/south-dakota/) - [Tennessee](https://isitonrecall.com/state/tennessee/) - [Texas](https://isitonrecall.com/state/texas/) - [Utah](https://isitonrecall.com/state/utah/) - [Virginia](https://isitonrecall.com/state/virginia/) - [Vermont](https://isitonrecall.com/state/vermont/) - [Washington](https://isitonrecall.com/state/washington/) - [Wisconsin](https://isitonrecall.com/state/wisconsin/) - [West Virginia](https://isitonrecall.com/state/west-virginia/) - [Wyoming](https://isitonrecall.com/state/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. ## What to do next Customers who have affected product(s) should immediately review their inventory and quarantine all affected kits. Contact the Quality Department for further instructions on labeling and replacement product if needed at 406-259-6387. Customers will be provided with a label that is to be placed on the packs containing the recalled Medline Namic Angiogrphic (RA) 10CC Syringe. Aligned Medical Solutions is notifying its distributors by email and will arrange for labels to identify the packs with the recalled syringe. At the time the kit is opened for use any MEDLINE 10cc Syringe should be removed and destroyed. Customers with questions may contact the company via telephone at 1-800-360-9428 between the hours of 8:00 am and 5:00 pm (Mountain Time). Customers may also contact the company via email at fieldcorrectiveaction@alignedmedicalsolutions.com. [Read the current instructions](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/windstone-medical-packaging-dba-aligned-medical-solutions-issues-nationwide-recall-namic) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Windstone Medical Packaging dba Aligned Medical Solutions records](https://isitonrecall.com/brand/windstone-medical-packaging-dba-aligned-medical-solutions/)