Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K132804 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ACUSON S 1000, ACUSON S 2000, or ACUSON S 3000 ultrasound systems with software version C3, C3, C3,... | 2 | 07/29/2015 | Siemens Medical Solutions USA, Inc. |
ACUSON S Family Ultrasound Systems at software versions VC25D, VC30A and VC30B; (S2000, S3000 and S1... | 2 | 07/01/2014 | Siemens Medical Solutions USA, Inc. |
ACUSON S2000 and ACUSON S3000 ultrasound systems with the Virtual Touch IQ option; Model numbers: ... | 2 | 07/30/2015 | Siemens Medical Solutions USA, Inc. |
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