# FDA recall Z-2370-2026

> **ARROW INTERNATIONAL, LLC** · Class I · device recall initiated 2026-04-21.

## Product

Description/REF:  PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS  AGBA PICC/DELTA: 2L 5.5 FR X 50 CM/ASK-45052-NS  AGBA PICC/DELTA KIT: 1L 4.5 FR X 55 CM/ASK-45541-MHBV  PICC KIT: 2L 5.5 FR X 55 CM CG+ VPS/ASK-45552-RH  AGBA PICC NaviCurve: 2L 5.5FR x 55CM BP/DLX-45552-CURVB  AGBA PICC NaviCurve: 2L 5.5FR x 55CM TCG/DLX-45552-CURVC  AGBA PICC: 2L 5.5FR x 55CM w Biopatch/DLX-45552-HPKB  AGBA PICC NaviCurve: 3L 6FR x 55CM BP/DLX-45563-CURVB  PI PICC KIT: 4 FR X 50 CM/ASK-35041-NH  PI PICC KIT: 2-L 5 FR X 50 CM/ASK-35052-NH  PI PICC G4 Stylet: 1L 4FR x 55CM w CHG/DLX-35541-VPSC  PI PICC NaviCurve: 2L 5FR x 55CM w BP/DLX-35552-CURVB  PI PICC NaviCurve: 3L 6FR x 55CM w BP/DLX-35563-CURVB  PI PICC G4 Stylet: 3L 6FR x 55CM w BP/DLX-35563-VPSB  AGBA PI PICC KIT: 2L 5.5 FR X 55CM/CDC-45552-HPK1A  PI AGBA PICC KIT: 3-L 6 FR X 55 CM/CDC-45563-HPK1A  PI AGBA PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-UOI1  PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-VFH1  PI AGBA PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-UOI1  PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-VFH1  PI AGBA PICC KIT: 3L 6 FR X 55 CM W/VPS/ASK-45563-UWH1  AGBA PICC NaviCurve: 1L 4.5FR x 55CM BP/DLX-45541-CURVB  AGBA PICC NaviCurve: 1L 4.5FR x 55CM TCG/DLX-45541-CURVC  AGBA PICC G4 Stylet: 1L 4.5FR x 55CM TCG/DLX-45541-VPSC  AGBA PICC G4 Stylet: 2L 5.5FR x 55CM BP/DLX-45552-VPSB  AGBA PICC G4 Stylet: 2L 5.5FR x 55CM TCG/DLX-45552-VPSC  PI PICC:1L 4FR X 50CM PRELOAD VPS STYLET/CDC-35041-VPS  PICC KIT: 3 FR X 55 CM/CDC-05531-PK1A

## Reason for recall

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.

## 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.

## Key facts

- **Recall number:** Z-2370-2026
- **Recalling firm:** ARROW INTERNATIONAL, LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-21
- **Report date:** 2026-06-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2370-2026

## Citation

> MORVS. FDA recall Z-2370-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-2370-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*