Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K922637 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Y-Type Blood, Outlook Pump Set, Caresite-single-use for use with the Outlook Safety Infusion System ... | 2 | 09/24/2021 |
FEI # 2523676 B. Braun Medical, Inc. |
| Outlook Pump Primary Administration Set w/ micro Tubing for Epidural Administration-single use, for ... | 2 | 09/24/2021 |
FEI # 2523676 B. Braun Medical, Inc. |
| Outlook Pump Y Type Blood Set with 170um Blood Filter, Injection Site, Spin Lock Connector, 131 in | 2 | 01/26/2010 |
FEI # 2523676 B. Braun Medical, Inc. |
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