Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Arrow EZ-IO Needle Set 45 mm 15 ga Recalled by Teleflex Medical Due to Some of the individual unit packaging (pouches) may...

Date: March 29, 2017
Company: Teleflex Medical
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Teleflex Medical directly.

Affected Products

Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.

Quantity: 4760 eaches

Why Was This Recalled?

Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.

Where Was This Sold?

This product was distributed to 48 states: AL, AK, AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY

Affected (48 states)Not affected

About Teleflex Medical

Teleflex Medical has 204 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report