Arrow IPN037402

• FDA 510(k) K121403 decided 20 Jun 2012 Active
• FDA GUDID UDI-DI 10801902125092 listed 30 Sep 2016 Listed

• • Ongoing Z-2364-2026 FDA Class I ·initiated 21 Apr 2026

  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.

• 3 recalls, same reason

  • Terminated Z-1253-2020 FDA Class II ·initiated 20 Dec 2019
  • Terminated Z-1241-2020 FDA Class II ·initiated 20 Dec 2019
  • Terminated Z-1239-2020 FDA Class II ·initiated 20 Dec 2019

  Product lidstock contains the incorrect expiration date for the product

• • Terminated Z-1958-2018 FDA Class II ·initiated 11 Apr 2018

  Product sterility may be compromised due to unsealed packaging.

• • Terminated Z-0573-2015 FDA Class II ·initiated 10 Nov 2014

  Arrow is recalling certain lots of the Continuous Nerve Block Component, Product Code: AB-18040-N, due to a labeling inconsistency. The product lidstock incorrectly identifies the needle in the finished good as 17Ga rather than the correct 18Ga. The product included in the package is the correct 18Ga size. No injuries or illnesses have been reported.

• • Terminated Z-0546-2014 FDA Class II ·initiated 9 Oct 2013

  A labeling inconsistency was discovered in which the lidstock states that the kit contains a stimulator cable with 1.5mm socket, however, the kit contains a stimulator cable with 1.5mm pin.

1. 20 Jun 2012 Cleared FDA 510(k) K121403
2. 9 Oct 2013 Recall initiated FDA recalls Z-0546-2014
3. 10 Nov 2014 Recall initiated FDA recalls Z-0573-2015
4. 30 Sep 2016 Listed FDA GUDID 10801902125092
5. 11 Apr 2018 Recall initiated FDA recalls Z-1958-2018
6. 20 Dec 2019 Recall initiated FDA recalls Z-1253-2020
7. 20 Dec 2019 Recall initiated FDA recalls Z-1241-2020
8. 20 Dec 2019 Recall initiated FDA recalls Z-1239-2020
9. 21 Apr 2026 Recall initiated FDA recalls Z-2364-2026

Trade name

Arrow

Generic name

Peripheral anaesthesia catheter set, non-medicated

Model / Ref / Catalog

IPN037402, ASK-19608-CC

Primary DI / UDI-DI

10801902125092

510(k) Number

K121403 ↗

FDA product code

CAZ

GMDN term

Peripheral anaesthesia catheter set, non-medicated

Device class

Class II

Regulation number

868.5140

GUDID distribution status

In Commercial Distribution

Category: Peripheral anaesthesia catheter set, non-medicated

Other devices filed under FDA product code CAZ (Anesthesia conduction kit).

• B-SMART, MODEL B-01 by Macosta Medical USA, LLC
• MORE-L INJECTOR KIT PLUS by Incutech, Inc.
• PANDIN CONTINUOUS NERVE STIMULATING CATHETER, MODELS 561-18-05, 561-18-09, 561-18-15, 562-18-05, 562-18-09 & 562-18-15 by Hdc Corp.
• EPIDURAL CATHETER MODELS 1210/1200 by Rusch Intl.
• PERIPHERAL NERVE BLOCK SUPPORT TRAY by Life-Tech Intl., Inc.
• MEDTRONIC EPIDURAL CATHETER KIT MODEL 8716 by MEDTRONIC VASCULAR, INC.
• MICOR ANESTHESIA CONDUCTION KIT by Micor, Inc.
• B-D LOSS OF RESISTANCE SYRINGE by Bd Becton Dickinson Vacutainer Systems Preanalytic
• CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET by Teleflex LLC
• PERFIX SET FOR EPIDURAL ANESTHESIA W/TUO by Burron Medical Products, Inc.

• Arrow IPNB00820 Open recall

  Class II

  FDA 510(k) K140110 Active Cleared 27 Mar 2015 GUDID on market

• Arrow IPNB00826 Open recall

  Class II

  FDA 510(k) K140110 Active Cleared 27 Mar 2015 GUDID on market

• Arrow IPNB00822 Open recall

  Class II

  FDA 510(k) K140110 Active Cleared 27 Mar 2015 GUDID on market

• Arrow IPNB00827 Open recall

  Class II

  FDA 510(k) K140110 Active Cleared 27 Mar 2015 GUDID on market

See all devices from Teleflex Incorporated →