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Biim Ultrasound L12-4 Linear Array Transducer (Version P2.0)

Biim Ultrasound AS · Model P001000-04 · UDI-DI 07090045490365

IYOITXLLZ Prescription
1
510(k) clearances
6,553
Adverse events (17 deaths)
82
Recalls
350
Facilities

Description

Biim Ultrasound L12-4 Linear Array Transducer (Version P2.0)

Recalls

DateFirmReason
2026-03-02Civco Medical Instruments Co. Inc.There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified
2026-03-02Civco Medical Instruments Co. Inc.There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified
2026-03-02Civco Medical Instruments Co. Inc.There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified
2026-03-02Civco Medical Instruments Co. Inc.There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified
2026-03-02Civco Medical Instruments Co. Inc.There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified
2026-03-02Civco Medical Instruments Co. Inc.There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified
2026-03-02Civco Medical Instruments Co. Inc.There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified
2026-03-02Civco Medical Instruments Co. Inc.There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified
2022-01-24Volcano CorpMulti-Modality Touch Screen Modules (MM-TSM), which are bedside/secondary control units, used as part of Mobile IVUS systems, are missing the following labeling information: Unique
2021-11-04GE Healthcare, LLCThe firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connec

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.