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-1203-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code JC-05400-E | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1193-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code CA-02220 | 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-1182-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05503-BID | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1180-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05501-SH | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1176-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05500-TM | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1179-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05400-CA1 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1174-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRH | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1172-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code AK-05501 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1177-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code AK-05500 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
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