FDA Device recall Z-1829-2017
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079
- FDA Device
- Class III
- terminated
- Published 2017-04-26
On 2017-04-26 the FDA classified a Class III recall of Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079 by Teleflex Medical, citing some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1829-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-03-29 |
| Published | 2017-04-26 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Teleflex Medical |
| Distribution | AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
Product
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Reason
Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
Identifiers
| code_info | 4799431 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1829-2017%22
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