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-1170-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1218-2020 - EPIDURAL CATHETERIZATION KIT, Product Code BJC-05400-BEN | 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-1173-2020 - EPIDURAL CATHETERIZATION KIT, Product Code ALZANO-05400-B | 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-1175-2020 - TheraCath Epidural Catheterization Kit, Product Code ASK-05001-SLR1 | 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-1177-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code AK-05500 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1178-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05500-BID | 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 |
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