RecallRadar

FDA Device recall Z-0677-2021

IceEDGE" 2.4¿ 90p¿ Cryoablation Needle

On 2020-12-30 the FDA classified a Class II recall of IceEDGE" 2.4¿ 90p¿ Cryoablation Needle by Boston Scientific, citing complaint trend regarding needle shaft gas leaks.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0677-2021
ClassificationClass II
Statuscompleted
Initiated2020-11-18
Published2020-12-30
Last updated2026-09-13 11:55 UTC
CompanyBoston Scientific
DistributionUS

Product

IceEDGE" 2.4¿ 90p¿ Cryoablation Needle

Reason

Complaint trend regarding needle shaft gas leaks.

Identifiers

code_info
UPN: FPRPR3506 UDIs: 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 72901…UPN: FPRPR3506 UDIs: 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594, 7290104830594 Batch Numbers: U0288, U0287, U0062, U0060, T0433, T0434, T0416, T0417, X6836, A6781, A6782, A6762, A6761, A2078, A2079, A1529, A1373, A1374

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: completed.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0677-2021%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.