Windstone Medical Packaging Recalls Custom Convenience Kits
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Windstone Medical Packaging, Inc. is recalling 150 Custom Convenience Kits containing Medline Namic RA Syringes due to risk of adapter disconnection.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on June 2, 2026 and geographically references Arizona. Its severity classification of "high" 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. initiated a voluntary recall of Custom Convenience Kits after determining they contain Medline Namic Angiographic Control Syringes with Rotating Adapter that may have a rotating adapter unwind during use.
Which Products Are Affected
The recall affects 150 kits distributed in Arizona with the following details:
- Angio Pack Part numbers: AMS6908E, AMS6908F
- Pack AMS6908E: UDI-DI B098AMS6908E0, Lot 214875
- Pack AMS6908F: UDI-DI B098AMS6908F0, Lots 215436, 225001, 226706, 234088 Recall number Z-2066-2026. Classification: Class I.
What You Should Do
Consumers should stop using the affected kits and contact Windstone Medical Packaging, Inc. for further instructions.
Why This Matters
The defect creates a potential for biohazard exposure, blood loss, infection, or air embolism.
Source
FDA recall Z-2066-2026. 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 (901 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to June 2, 2026.
Frequently Asked Questions
Common questions about this FDA recall.