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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 of 49 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1180-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05501-SH 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-1182-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05503-BID 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-1184-2020 - FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-WH 2 01/24/2020 Arrow International Inc
Z-1185-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code ASK-17019-MSC 2 01/24/2020 Arrow International Inc
Z-1186-2020 - EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LEO 2 01/24/2020 Arrow International Inc
Z-1187-2020 - EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LIN 2 01/24/2020 Arrow International Inc
Z-1188-2020 - EPIDURAL CATHETERIZATION KIT, Product Code BE-05400B-ETTEL 2 01/24/2020 Arrow International Inc
Z-1189-2020 - EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCHH 2 01/24/2020 Arrow International Inc
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