Arrow International Inc: Medical Device Recall in 2020 - (Recall #: Z-0844-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Arrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018" (0.46 mm) dia. Spring-Wire Guide Product Code: ASK-04020-PMC The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels.

Product Classification:

Class II

Date Initiated: December 12, 2019

Date Posted: January 29, 2020

Recall Number: Z-0844-2020

Event ID: 84635

Reason for Recall:

The lidstock label incorrectly displays a MR (Magnetic Resonance ) Conditional symbol (instead of a MR Unsafe symbol) in reference to a component of the kit

Status: Ongoing

Product Quantity: 80 eaches

Code Information:

Lot/Batch Number: PMC 23F19H0224

Distribution Pattern:

US distribution to SC

Voluntary or Mandated:

Voluntary: Firm initiated