Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-2395-2026Class I

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

Arrow International LLC (subsidiary of Teleflex Incorporated) / initiated 2026-04-21 / Open, Classified / root cause: manufacturing process

ARROW INTERNATIONAL, LLC began a recall of Description/REF: PICC ACCESS TRAY/ASK-04001-CG1 on . FDA classified it as Class I and gives the reason as "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...". As of , the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-2395-2026
Classification
Class I
Status
Open, Classified
Initiated
Posted
Recalling firm
Arrow International LLC (subsidiary of Teleflex Incorporated)
Product
Description/REF: PICC ACCESS TRAY/ASK-04001-CG1
Product code
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
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.
Root cause tag
manufacturing process
FDA root cause
Nonconforming Material/Component
Action
On 4/21/2026, correction notices (Firm Event Number: EIF-000608, lidocaine and bupivacaine) were mailed to customers who were asked to do the following: Arrow International LLC is voluntarily recalling product due to the Huons Co. Ltd. recall of Lidocaine and Bupivacaine, which is included in impacted Arrow Kits & Sets. Medical facilities 1. Provide this correction notice to all persons who need to be aware within your organization or to any organization where the potentially affected product has been transferred. 2. Check your inventory for product within the scope of this Medical Device Notification and place a copy of this notice with all affected product. 3. Complete and return the response form virtually via: https://fca.myteleflex.com/en/recall/000608 Distributors: 1. Provide Medical Device Notification to all customers who have received impacted product. Each of your customers is then required to complete the Acknowledgement Form and return it to you as their distributor. 2. Check your inventory for affected product. Place a copy of this notification with all affected product and ensure that the notification is included with future distributions of affected product. 3. Complete and return the response form via link: https://fca.myteleflex.com/en/recall/000608 4. If you have further distributed product outside of your country, please notify Teleflex Customer Service by return email. If you have questions contact firm's Customer Service: Link: https://fca.myteleflex.com/en/recall/000608, Customer Service: Telephone: 1-866-396-2111, FAX: 1-855-419-8507 Email: [email protected] On 5/29/2026, additional amended notices (Firm Event Number: EIF-000608-01) were mailed to include additional affected devices. On 5/1/2026, additional notices (Firm Event Number: EIF-000609, sodium chloride) were mailed and emailed to customers who have 0.9% sodium chloride (10mL saline solution ampule) in kits and sets.
Quantity in commerce
360
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.
Product codes and lots
REF(Material)/UDI-DI/Lot(Batch): ASK-04001-CG1/10801902193275/33F25C0224, 33F25D0647, 33F25G0390, 33F25J0348

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2395-2026
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-2363-2026Class IOngoingVoluntary: Firm initiated
Z-2364-2026Class IOngoingVoluntary: Firm initiated
Z-2365-2026Class IOngoingVoluntary: Firm initiated
Z-2366-2026Class IOngoingVoluntary: Firm initiated
Z-2367-2026Class IOngoingVoluntary: Firm initiated
Z-2368-2026Class IOngoingVoluntary: Firm initiated
Z-2369-2026Class IOngoingVoluntary: Firm initiated
Z-2370-2026Class IOngoingVoluntary: Firm initiated
Z-2371-2026Class IOngoingVoluntary: Firm initiated
Z-2372-2026Class IOngoingVoluntary: Firm initiated
Z-2373-2026Class IOngoingVoluntary: Firm initiated
Z-2374-2026Class IOngoingVoluntary: Firm initiated
Z-2375-2026Class IOngoingVoluntary: Firm initiated
Z-2376-2026Class IOngoingVoluntary: Firm initiated
Z-2377-2026Class IOngoingVoluntary: Firm initiated
Z-2378-2026Class IOngoingVoluntary: Firm initiated
Z-2379-2026Class IOngoingVoluntary: Firm initiated
Z-2380-2026Class IOngoingVoluntary: Firm initiated
Z-2381-2026Class IOngoingVoluntary: Firm initiated
Z-2382-2026Class IOngoingVoluntary: Firm initiated
Z-2383-2026Class IOngoingVoluntary: Firm initiated
Z-2384-2026Class IOngoingVoluntary: Firm initiated
Z-2385-2026Class IOngoingVoluntary: Firm initiated
Z-2386-2026Class IOngoingVoluntary: Firm initiated
Z-2387-2026Class IOngoingVoluntary: Firm initiated
Z-2388-2026Class IOngoingVoluntary: Firm initiated
Z-2389-2026Class IOngoingVoluntary: Firm initiated
Z-2390-2026Class IOngoingVoluntary: Firm initiated
Z-2391-2026Class IOngoingVoluntary: Firm initiated
Z-2392-2026Class IOngoingVoluntary: Firm initiated
Z-2393-2026Class IOngoingVoluntary: Firm initiated
Z-2394-2026Class IOngoingVoluntary: Firm initiated
Z-2395-2026Class IOngoingVoluntary: Firm initiated
Z-2396-2026Class IOngoingVoluntary: Firm initiated
Z-2397-2026Class IOngoingVoluntary: Firm initiated