fda
4 records
FDA Device Recall: VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref. Number: 108910
2018-09-19
Class II — Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver
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FDA Device Recall: 07-150-07 MIZUHO, MAL DISP DOPPLER PROBE BX 4, REF 138200 The Doppler probe i
2014-07-16
Class II — Report of the product penetrating the sterile barrier; this could render the product unsterile.
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FDA Device Recall: 07-150-10 MIZUHO, DOPPLER PROBE, SLIM, BX 4, REF 138660 The Doppler probe is
2014-07-16
Class II — Report of the product penetrating the sterile barrier; this could render the product unsterile.
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FDA Device Recall: 07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe
2014-07-16
Class II — Report of the product penetrating the sterile barrier; this could render the product unsterile.
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nppes
1 records
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