Arrow International Recalls PI MIDLINE 2L Kits
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ARROW INTERNATIONAL, LLC is recalling 90 units of PI MIDLINE 2L kits distributed nationwide due to inclusion of recalled drugs that may compromise sterility.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 2, 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
ARROW INTERNATIONAL, LLC initiated a voluntary recall of certain midline catheter kits after a supplier recall of Lidocaine, Bupivacaine, and 0.9% sodium chloride included in the kits. The supplier had quality issues with limited reports of drug ineffectiveness. Compromised sterility of water-based injectable products could lead to serious or life-threatening injuries.
Which Products Are Affected
- Product: PI MIDLINE 2L: 5FR X 20CM
- REF: CDC-32052-MPKC
- UDI-DI/Lot: 10801902193275/33F24L0236
- Quantity: 90 units
- Distribution: US Nationwide including VA, NY, UT, SC, LA, MN, PA, AZ, CA, MI, OH, FL, CT, KS, IL, TX, WI, GA, NC, MD, OR, AK, NH, IA, ND, OK, NM, AL, MA, KY, WA, AR, CO, IN, ME, TN, WY, NJ, SD, MS, MO, MT, DE, ID, NE, WV, RI, VT, NV, HI, DC, PR
- Recall Number: Z-2387-2026
- Classification: Class I
What You Should Do
Consumers and healthcare facilities should check inventory for the affected lots and follow instructions provided in the firm's notification letter for returns or further guidance. Contact ARROW INTERNATIONAL, LLC for additional information on the recall.
Why This Matters
This Class I recall addresses a situation where compromised sterility could result in serious or life-threatening injuries from use of the affected kits.
Source
FDA recall Z-2387-2026, report date 20260624
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 (1,352 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 2, 2026.
Frequently Asked Questions
Common questions about this FDA recall.