Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-1829-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class III

Date Initiated: March 29, 2017

Date Posted: April 26, 2017

Recall Number: Z-1829-2017

Event ID: 76872

Reason for Recall:

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

Status: Terminated

Product Quantity: 4760 eaches

Code Information:

4799431

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated