RecallRadar

FDA Device recall Z-1958-2018

Continuous Nerve Block Needle

On 2018-06-06 the FDA classified a Class II recall of Continuous Nerve Block Needle by Arrow International, citing product sterility may be compromised due to unsealed packaging.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1958-2018
ClassificationClass II
Statusterminated
Initiated2018-04-11
Published2018-06-06
Last updated2026-09-13 11:54 UTC
CompanyArrow International
DistributionUS

Product

Continuous Nerve Block Needle; Product Codes: AB-00090, AB-00150, AB-17040-N, AB-17080-N, AB-17110-N, AB-17140-N, AB-18080-N, AB-18110-N

Reason

Product sterility may be compromised due to unsealed packaging.

Identifiers

code_info
Lot Numbers: 13F17G0253 13F17A0200 13F17F0505 13F17G0256 13F17J0455 13F17C0193 13F17K0105 13F17C0198 13F17J02…Lot Numbers: 13F17G0253 13F17A0200 13F17F0505 13F17G0256 13F17J0455 13F17C0193 13F17K0105 13F17C0198 13F17J0280 13F17A0063 13F17A0061 13F17B0252 13F17F0190 13F17L0701 13F17A0064 13F17C0225 13F17D0342 13F17J0229 13F17K0592 13F17M0002 13F17A0201 13F17D0246

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-1958-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.