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

Recall date

March 29, 2017

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1829-2017

FDA classification

Class III

Brand / firm

Teleflex Medical

Sold / distributed

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, Canada and Costa Rica

Why it was recalled

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

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

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