Fresh Recalls

FDAClass II · Medical device · Recall Z-2815-2026 · Recalled August 5, 2026

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as recall — Windstone Medical Packaging, Inc.

Agency report date: August 5, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as
Company / brand
Windstone Medical Packaging
Lot / serial / date codes
UDI/DI B098AMS94610, Lot Numbers: 230658, 231173.
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.
Agency product description and boundaries

AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: Angio Pack - RX, Part Number AMS9461

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as

3. Open the official notice or contact

Official recall ID
Z-2815-2026
Brand
Windstone Medical Packaging
Classification
Class II
Units affected
60 kits
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Billings, MT, United States
Firm address
1602 4th Ave N, N/A, 59101-1521

Identifying details (verbatim from the notice)

Product codes / lots
UDI/DI B098AMS94610, Lot Numbers: 230658, 231173.
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.
Firm notified the public via
E-Mail
FDA event ID
99347
Recall initiated
June 17, 2026
FDA classified
July 27, 2026
FDA report date
August 5, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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