Halyard PERC TRAY Kit Recall Issued
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AVID Medical, Inc. is recalling 6,052 Halyard PERC TRAY kits due to a potential disconnection risk with the syringe adaptor.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 26, 2026 and geographically references United States. 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, Devices.
What Happened AVID Medical, Inc. initiated a voluntary recall of Halyard PERC TRAY kits because of a potential risk for the Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Which Products Are Affected The recall involves Halyard PERC TRAY kits with model numbers SLPC34-01 and SLPC34-02. A total of 6,052 kits are affected. Distribution was limited to FL, IL, MO, MS, NC, NE, and TX. Specific lot details are available under recall number Z-1977-2026.
What You Should Do No specific consumer instructions are provided in the recall notice.
Why This Matters This is a Class I recall, indicating a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
Source FDA Recall Z-1977-2026 - AVID Medical, Inc., Toano, VA
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 (970 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to May 26, 2026.
Frequently Asked Questions
Common questions about this FDA recall.