AMS Block Tray Medical Kits Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Windstone Medical Packaging is recalling 100 AMS ALIGNED MEDICAL SOLUTIONS Block Tray convenience kits containing Lidocaine HCl due to supplier quality issues.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 13, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
Windstone Medical Packaging, Inc. issued a recall for specific lots of AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits containing Elevaris Lidocaine HCl injection USP. The action follows a recall of the Lidocaine HCl injection USP by Elevaris Medical Devices Inc. due to supplier quality issues.
Which Products Are Affected
The recall covers AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as Block Tray - RX, Part Number AMS12414. Affected products have UDI/DI B098AMS124140 and Lot Number 230411. A total of 100 kits were distributed nationwide 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, and WA. The FDA recall number is Z-2817-2026.
What You Should Do
Consumers should stop using the affected kits and contact Windstone Medical Packaging, Inc. for return or refund instructions.
Why This Matters
The Class II recall addresses potential quality issues with a component in the kits that could lead to temporary or reversible adverse health consequences.
Source
FDA recall Z-2817-2026; https://www.fda.gov
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,118 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 13, 2026.
Frequently Asked Questions
Common questions about this FDA recall.