Z-1829-2017 Class III Terminated
FDA device recall Z-1829-2017 was initiated by Teleflex Medical on March 29, 2017 and is designated Class III. Reason for recall: Some of the individual unit packaging (pouches) may be missing the lot number an expiration date. The recall status is terminated (terminated April 19, 2024). Affected quantity: 4760 eaches.
Recall Details
- Product Type
- Devices
- Report Date
- April 26, 2017
- Initiation Date
- March 29, 2017
- Termination Date
- April 19, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4760 eaches
Product Description
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.
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
Code Information
4799431