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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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Z-1190-2020 - EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCSHO 2 01/24/2020 FEI # 3015859709
Arrow International Inc
Z-1191-2020 - EPIDURAL CATHETERIZATION KIT, Product Code BE-080180-BXL 2 01/24/2020 FEI # 3015859709
Arrow International Inc
Z-1192-2020 - EPIDURAL CATHETERIZATION KIT, Product Code BE-080180-CHH 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-1194-2020 - EPIDURAL CATHETERIZATION KIT, Product Code CZ-05400-EPI 2 01/24/2020 FEI # 3015859709
Arrow International Inc
Z-1195-2020 - EPIDURAL CATHETERIZATION KIT, Product Code DE-05400D-BO 2 01/24/2020 FEI # 3015859709
Arrow International Inc
Z-1196-2020 - FlexTip Plus Epidural Catheterization Set for Pediatric Lumbar Placement, Product Code EC-05520-P 2 01/24/2020 FEI # 3015859709
Arrow International Inc
Z-1197-2020 - EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-04 2 01/24/2020 FEI # 3015859709
Arrow International Inc
Z-1198-2020 - EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-10 2 01/24/2020 FEI # 3015859709
Arrow International Inc
Z-1199-2020 - EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-12 2 01/24/2020 FEI # 3015859709
Arrow International Inc
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