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-1180-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05501-SH | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1181-2020 - Epidural Catheterization Kit with FlexTip Plus, Open Tip, Single- Port Catheter, Product Code ASK-05502-NY | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1182-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05503-BID | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1183-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-TG1 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1184-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-WH | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1185-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-17019-MSC | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1186-2020 - EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LEO | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1187-2020 - EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LIN | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1188-2020 - EPIDURAL CATHETERIZATION KIT, Product Code BE-05400B-ETTEL | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1189-2020 - EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCHH | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
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