Medical Device Recalls
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Related Medical Device Recalls |
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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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| Z-1210-2020 - EPIDURAL CATHETERIZATION KIT, Product Code MTO-09903-KU | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1211-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code NYU-05500-1 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1212-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code TI-05501-ME | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1213-2020 - Epidural Catheterization Kit with FlexTip Plus Catheter, Product Code TI-05520-EPI | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1214-2020 - EPIDURAL CATHETERIZATION KIT, Product Code UR-05501 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1215-2020 - EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-EXP | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1216-2020 - EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-FR1 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1217-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code YC-02220 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1171-2020 - FlexTip Plus Epidural Catheterization Set, Product Code AA-05400-E | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
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