fda
2 records
FDA Device Recall: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device Mode
2015-04-29
Class II — TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be delivered and may cause: stricture,scarring, bradycardia, or pneumothorax
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FDA Device Recall: CSA Medical truFreeze System; Model: CC3-01, a cryogenic surgical device ***T
2015-01-14
Class II — An increase in complaint trending for a loss of audible sound associated with the timer has been observed.
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nppes
1 records
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