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very recent recall may be missing. Everything shown is accurate as of the last checked time on this page —
for anything time-critical, confirm with the official sources linked below.
FDAClass I · Medical device · Recalled June 24, 2026
Description/REF recall — ARROW INTERNATIONAL, LLC
Hazard: Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Class I: most serious — reasonable probability of serious health consequences or death.
View the official FDA enforcement record (openFDA) ↗
- Official recall ID
- Z-2387-2026
- Brand
- ARROW INTERNATIONAL
- Classification
- Class I
- Units affected
- 90
- Recall status
- Ongoing
- Initiated
- Voluntary: Firm initiated
Description
Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC
Affected products
Companies & origin
- Recalling firm location
- Morrisville, NC, United States
- Firm address
- 3015 Carrington Mill Blvd, 27560-5437
Identifying details (verbatim from the notice)
- Product codes / lots
- REF(Material)/UDI-DI/Lot(Batch): CDC-32052-MPKC/10801902193275/33F24L0236
- Distribution
- US Nationwide distribution including in the states of 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.
- Firm notified the public via
- Letter
- FDA event ID
- 98793
- Recall initiated
- April 21, 2026
- FDA classified
- June 12, 2026
- FDA report date
- June 24, 2026
Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim;
the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.
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