Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K122767 |
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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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BIOFLO 8F SINGLE TITANIUM NON- FILLED; VALVED, UPN H965440250, Cat. No. 44-025 - Product Usage: Long... | 2 | 11/21/2019 | Angiodynamics Inc. (Navilyst Medical Inc.) |
BIOFLO 8F SINGLE PLASTIC FILLED; NON-VALVED, UPN H965440140, Cat. No. 44-014 - Product Usage: Long-t... | 2 | 11/21/2019 | Angiodynamics Inc. (Navilyst Medical Inc.) |
XCELA, 8F SINGLE PLASTIC PORT FILLED, VALVED, UPN H965440400, Cat. No. 44-040 - Product Usage: Long-... | 2 | 11/21/2019 | Angiodynamics Inc. (Navilyst Medical Inc.) |
BIOFLO 8F SINGLE PLASTIC NON-FILLED; VALVED, UPN H965440210, Cat. No. 44-021 - Product Usage: Long-t... | 2 | 11/21/2019 | Angiodynamics Inc. (Navilyst Medical Inc.) |
BIOFLO 8F SINGLE PLASTIC FILLED; VALVED, UPN H965440220, Cat. No. 44-022 | 2 | 11/21/2019 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Port Kit with Access Infusion Set under the following labels: 1) 8F/SL/Plastic Port/F, Product Numbe... | 2 | 01/24/2014 | Navilyst Medical, Inc. |
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