Arrow EZ-IO Needle Set 45 mm 15 ga — Class III medical device recall Z-1829-2017
Terminated recall by Teleflex Medical, reported 2017-04-26, distributed in AK, AL, AR, AZ, CA, CO, CT, FL…. Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
| Recall number | Z-1829-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2017-03-29 |
| Classified | 2017-04-15 |
| Reported by FDA | 2017-04-26 |
| Terminated | 2024-04-19 |
| Distributed | 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 |
| Countries outside the US | CA, CR |
| Quantity | 4,760 eaches |
| Model numbers | 9079 |
Product
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Reason for recall
Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1829-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.