RecallRadar

FDA Device recall Z-2056-2025

Philips L8-4 Transducer

On 2025-07-09 the FDA classified a Class II recall of Philips L8-4 Transducer by Philips Ultrasound, citing ultrasound transducer devices were refurbished beyond their useful life.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2056-2025
ClassificationClass II
Statusongoing
Initiated2025-05-28
Published2025-07-09
Last updated2026-09-13 11:57 UTC
CompanyPhilips Ultrasound
DistributionUS

Product

Philips L8-4 Transducer.

Reason

Ultrasound transducer devices were refurbished beyond their useful life.

Identifiers

code_info
Model No. 989605440811, 989605440812; UDI: (01)00884838067684(21)B0LZNN, (01)00884838067684(21)03BPVM, (01)008848380676…Model No. 989605440811, 989605440812; UDI: (01)00884838067684(21)B0LZNN, (01)00884838067684(21)03BPVM, (01)00884838067684(21)02KMFZ, (01)00884838067684(21)02HJDK, (01)00884838067684(21)02FWNQ, (01)00884838067684(21)02KKZT, (01)00884838067684(21)03H7GL, (01)00884838067684(21)02LTKK, (01)00884838067684(21)02H2JM, (01)00884838067684(21)02KKVB, (01)00884838067684(21)038XYV, (01)00884838067684(21)02DLVR, (01)00884838067684(21)02CCM5, (01)00884838067684(21)02LT6G, (01)00884838067684(21)02KMKK, (01)00884838067684(21)02V8VD, (01)00884838067684(21)037Z2B, (01)00884838067684(21)02NK5J; Serial No. B0LZNN, 03BPVM, 02KMFZ, 02HJDK, 02KLBP, 02FWNQ, 02RTF9, 02KKZT, 03H7GL, 02LTKK, 02H2JM, 02KKVB, 038XYV, 02H34T, 02DLVR, 02CCM5, 02LT6G, 02KMKK, 02V8VD, 02JC66, 02V016, 037Z2B, 02NK5J.

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-2056-2025%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.