Recall of Arrowg+ard Blue MAC Two-Lumen Central Venous Access Kit
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
ARROW INTERNATIONAL, LLC is voluntarily recalling 95 units of the Arrowg+ard Blue MAC Two-Lumen Central Venous Access Kit due to incorrectly manufactured liquid adhesive, affecting distribution in specific U.S. states.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 8, 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, cpsc, Devices.
What Happened
The recall was initiated due to a notice from a supplier that the liquid adhesive in the product was incorrectly manufactured.
Which Products Are Affected
The affected product is the Arrowg+ard Blue™ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters, with REF ASK-21142-DMC, UDI code (01)10801902218930(17)270630(11)251211(10)33F25M0671, and Batch Number 33F25M0671. Approximately 95 units are affected, distributed in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA, as part of U.S. nationwide distribution. The official recall number is Z-1917-2026.
What You Should Do
Consumers should contact the recalling firm, ARROW INTERNATIONAL, LLC, at 3015 Carrington Mill Blvd, Morrisville, NC 27560-5437, as the recall was initiated via letter notification for further instructions on returns or refunds.
Why This Matters
This recall involves medical devices used for short-term venous access, which could impact patient safety due to manufacturing issues.
Source
FDA recall notice: Z-1917-2026
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 (1,048 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 8, 2026.
Frequently Asked Questions
Common questions about this FDA recall.