Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K801912 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Arrow TheraCath Epidural Catheter - Product Usage: The Arrow Epidural Catheter permits access to the... | 2 | 08/13/2020 | Arrow International Inc |
| Arrow EPIDURAL CATHETERIZATION KIT YC-02220 | 2 | 02/14/2020 | Arrow International Inc |
| Arrow EPIDURAL CATHETERIZATION KIT JH-05500 | 2 | 02/14/2020 | Arrow International Inc |
| Arrow® EPIDURAL CATHETERIZATION KIT AK-05000 | 2 | 02/14/2020 | Arrow International Inc |
| Arrow EPIDURAL CATHETERIZATION KIT AM-05500 | 2 | 02/14/2020 | Arrow International Inc |
| Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000 | 2 | 02/14/2020 | Arrow International Inc |
| Arrow EPIDURAL CATHETERIZATION KIT CK-02220 | 2 | 02/14/2020 | Arrow International Inc |
| TheraCath Epidural Catheterization Kit, Product Code ASK-05001-SLR1 | 2 | 01/24/2020 | Arrow International Inc |
| TheraCath(R) Epidural Catheter; Product Code: EC-05000 | 2 | 05/30/2018 | Arrow International Inc |
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