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-1200-2020 - EPIDURAL CATHETERIZATION KIT, Product Code IT-05400-DC | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1201-2020 - FlexTip Plus Epidural Catheterization Set, Product Code JC-05400-B | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1202-2020 - FlexTip Plus Epidural Catheterization Set, Product Code JC-05400-DCS | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1203-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code JC-05400-E | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1204-2020 - EPIDURAL CATHETERIZATION KIT, Product Code JC-05400-LB | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1205-2020 - 10 cc Luer-Slip Loss of Resistance Syringe, Product Code LR-05501 | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1206-2020 - FlexTip Plus Epidural Catheterization Set, Product Code MP-17019-TIP | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1207-2020 - FlexTip Plus Epidural Catheterization Kit, Product Code MP-17019-TKP | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1208-2020 - EPIDURAL CATHETERIZATION KIT, Product Code MTO-05500-SU | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
| Z-1209-2020 - FlexTip Plus Epidural Catheterization Set, Product Code MTO-05500-TK | 2 | 01/24/2020 |
FEI # 3015859709 Arrow International Inc |
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