AMS Aligned Medical Solutions Port Tray 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 15 AMS Port Tray medical convenience kits containing Lidocaine HCl injection 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, MedicalDevices.
What Happened
Windstone Medical Packaging, Inc. issued a recall for specific AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as Port Tray - RX after Elevaris Medical Devices Inc. recalled the contained Lidocaine HCl injection USP due to supplier quality issues.
Which Products Are Affected
The recall affects 15 kits of AMS ALIGNED MEDICAL SOLUTIONS Port Tray - RX, Part Number 008786-19, UDI/DI B098008786190, Lot Number 230451. Distribution was 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 recall number is Z-2819-2026.
What You Should Do
Consumers should contact the recalling firm for return or refund instructions. The recall was initiated voluntarily by the firm via E-mail on June 17, 2026.
Why This Matters
This Class II recall involves a medical device that may cause temporary or reversible adverse health consequences.
Source
FDA recall Z-2819-2026
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 (972 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.