Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K102543 |
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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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CF Delivery Dev Caps Bravo x5, FGS-0635/FGS 0636 - Product Usage: intended to be used for gastroesop... | 2 | 04/01/2021 | Covidien Llc |
BRAVO PH CAPS DELIVERY DEV5-PK, FGS-0312/FGS-0313 - Product Usage: intended to be used for gastroeso... | 2 | 04/01/2021 | Covidien Llc |
Bravo pH Monitoring capsule, UPC 7290101361695 (FGS# 0312) and UPC 7290101361688 (FGS# 0313). Pro... | 2 | 02/06/2012 | Given Imaging Ltd. |
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