RecallRadar

FDA Device recall Z-1548-2025

MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R

On 2025-04-16 the FDA classified a Class II recall of MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R by Medline Industries Northfield, citing medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1548-2025
ClassificationClass II
Statusongoing
Initiated2025-03-05
Published2025-04-16
Last updated2026-09-13 11:57 UTC
CompanyMedline Industries Northfield
DistributionUS

Product

MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R

Reason

Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

Identifiers

code_info
UDI/DI 10888277395374, Lot Numbers: 506894, 509420, 512983, 513469, 514448, 514549, 515557, 515860, 515903, 516550, 51…UDI/DI 10888277395374, Lot Numbers: 506894, 509420, 512983, 513469, 514448, 514549, 515557, 515860, 515903, 516550, 517359, 517626, 519259, 519413, 519966, 520277, 521360, 522144, 522145, 525472, 527111, 527115, 527121, 528456, 528457, 528582, 529483, 529485, 529487, 529489, 529930, 530432, 530433, 530434, 531020, 531024, 531676.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1548-2025%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.