Home/Recalls/FDA-Z-2395-2026
FDA DevicesClass I

Description/REF: PICC ACCESS TRAY/ASK-04001-CG1

Published: June 24, 2026Recall ID: Z-2395-2026Category: devicesCountry: US

Reason for Recall / 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.

Product Description & Identification

Description/REF: PICC ACCESS TRAY/ASK-04001-CG1

Additional Source Details

FieldValue
CityMorrisville
StateNC
Event id98793
Address 13015 Carrington Mill Blvd
Code infoREF(Material)/UDI-DI/Lot(Batch): ASK-04001-CG1/10801902193275/33F25C0224, 33F25D0647, 33F25G0390, 33F25J0348
Postal code27560-5437
Report date20260624
Product typeDevices
Product quantity360
Reason for recallLidocaine, 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.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260421
Initial firm notificationLetter
Center classification date20260612

Overview

  • Recalling FirmARROW INTERNATIONAL, LLC
  • StatusOngoing
  • Risk LevelClass I
  • DistributionUS 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.
Official Agency Alert