FDA Medical devices recall ·
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Port… recall
- Recall number
- Z-2819-2026
- Date
- (initiated June 17, 2026)
- Company / brand
- Windstone Medical Packaging, Inc.
1602 4th Ave N, Billings, MT, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 15 kits
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Port Tray - RX, Part Number 008786-19
Why was it recalled?
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to supplier quality issues.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI/DI B098008786190, Lot Numbers: 230451.
Distribution
US Nationwide distribution in the states of AZ, CA, CO, CT, FL, GA, IL, KS, LA, MA, MD, MN, MO, NH, NJ, NV, NY, OR, PA, TX, VA, WA.
States: Arizona California Colorado Connecticut Florida Georgia Illinois Kansas Louisiana Massachusetts Maryland Minnesota Missouri New Hampshire New Jersey Nevada New York Oregon Pennsylvania Texas Virginia Washington
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2819-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.