RecallRadar

FDA Device recall Z-2060-2025

Philips S7-3t Transducer

On 2025-07-09 the FDA classified a Class II recall of Philips S7-3t Transducer by Philips Ultrasound, citing ultrasound transducer devices were refurbished beyond their useful life.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2060-2025
ClassificationClass II
Statusongoing
Initiated2025-05-28
Published2025-07-09
Last updated2026-09-13 11:57 UTC
CompanyPhilips Ultrasound
DistributionUS

Product

Philips S7-3t Transducer.

Reason

Ultrasound transducer devices were refurbished beyond their useful life.

Identifiers

code_info
Model No. 989605440772, 989605440771, 989605439232, 989605406772, 989605439231, 989606708921, 989803002661; UDI: (01)00…Model No. 989605440772, 989605440771, 989605439232, 989605406772, 989605439231, 989606708921, 989803002661; UDI: (01)00884838061439(21)B2103Y, (01)00884838061439(21)B1J2M7, (01)00884838061439(21)B2HX4N, (01)00884838061439(21)B187KZ, (01)00884838061439(21)B2HXHR, (01)00884838061439(21)B2104Q, (01)00884838061439(21)B178YZ, (01)00884838061439(21)B22VWR, (01)00884838061439(21)B37JGY, (01)00884838061439(21)B131BH, (01)00884838061439(21)B3DVFC, (01)00884838061439(21)B1BX6R, (01)00884838061439(21)B3JQF5, (01)00884838061439(21)B1GVLN, (01)00884838061439(21)B1WBJZ, (01)00884838061439(21)B3QBXJ, (01)00884838061439(21)B1ZKPV, (01)00884838061439(21)F01W1D, (01)00884838061439(21)B34PDQ, (01)00884838061439(21)B2HX16, (01)00884838061439(21)B3JQFH, (01)00884838061439(21)B3JQQ4, (01)00884838061439(21)B3DV7C, (01)00884838061439(21)B2HWZV, (01)00884838061439(21)B3DV6Y, (01)00884838061439(21)B37JJC, (01)00884838061439(21)B210C8, (01)00884838061439(21)B2HXBW, (01)00884838061439(21)B1FKLQ, (01)0088483806143

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-2060-2025%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.