ClearanceBrief
Recall Z-2590-2023 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

ARROW INTERNATIONAL Inc.

Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular

DateSep 15, 2023 (initiated Aug 10, 2023)
StatusOpen, Classified
ReasonThis recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Root causeUnder Investigation by firm
ActionTeleflex/Arrow International issue an URGENT MEDICAL DEVICE RECALL notice on 08/10/2023 by FedEx 2nd day mail. The letter explained the problem, risk to patient, and requested the following actions: Medical facilities: Immediately cease use and distribution of affected product and quarantine for return. Distributors: Immediately cease use and distribution of affected product and quarantine for return. Provide a copy of this recall notice to all customers who have received impacted product. Request they complete the Acknowledgement Form and return it to you. Firm is requesting return
Quantity190 units
DistributionUS Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K073451PRESSURE INJECTABLE PICC
Arrow International, Inc., Jan 15, 2008