Halyard VA DETROIT CATH LAB PACK Kit Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
AVID Medical, Inc. is recalling 75 Halyard VA DETROIT CATH LAB PACK kits (model VMCD029) distributed to seven states due to potential syringe adaptor disconnection.
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, Medical Devices.
What Happened
AVID Medical, Inc. initiated a voluntary recall of Halyard VA DETROIT CATH LAB PACK 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 VA DETROIT CATH LAB PACK kits, model number VMCD029. Affected lot numbers are 1601753, 1601754, and 1621560 under UDI-DI 10809160388969. A total of 75 kits were distributed to FL, IL, MO, MS, NC, NE, and TX. The recall number is Z-1979-2026.
What You Should Do
The recall was initiated voluntarily by the firm via email notification on March 13, 2026. Consumers in possession of the affected kits should follow instructions provided by the recalling firm.
Why This Matters
This Class I recall involves a medical device where the hazard could lead to serious adverse health consequences.
Source
FDA recall Z-1979-2026
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 (984 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.