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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 49 Results
Related Medical Device Recalls
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Product Description
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Recall
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FDA Recall
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Z-1170-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B 2 01/24/2020 Arrow International Inc
Z-1211-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code NYU-05500-1 2 01/24/2020 Arrow International Inc
Z-1184-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-WH 2 01/24/2020 Arrow International Inc
Z-1183-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-TG1 2 01/24/2020 Arrow International Inc
Z-1178-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05500-BID 2 01/24/2020 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 Arrow International Inc
Z-1213-2020 - Epidural Catheterization Kit with FlexTip Plus Catheter, Product Code TI-05520-EPI 2 01/24/2020 Arrow International Inc
Z-1216-2020 - EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-FR1 2 01/24/2020 Arrow International Inc
Z-1215-2020 - EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-EXP 2 01/24/2020 Arrow International Inc
Z-1214-2020 - EPIDURAL CATHETERIZATION KIT, Product Code UR-05501 2 01/24/2020 Arrow International Inc
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