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-1957-2018 - Catheter Hemostasis Valve For use with .038" (.096 cm) dia. and smaller guide wires; Product Code: AI-07000 | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Z-1958-2018 - Continuous Nerve Block Needle; Product Codes: AB-00090, AB-00150, AB-17040-N, AB-17080-N, AB-17110-N, AB-17140-N, AB-18080-N, AB-18110-N | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Z-1959-2018 - Echogenic Introducer Needle; Product Code: AN-04318 | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Z-1960-2018 - Spring Wire Guide Introducer Needle; Product Codes: AN-04320 and AN-04418 | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Z-1961-2018 - Epidural Needle; Product Codes: AN-05501 and AN-05505 | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Z-1962-2018 - SnapLock" Catheter/Syringe Adapter; Product Code: AS-05500 | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Z-1963-2018 - Maximal Barrier Drape; Product Codes: ASK-00001-1A | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Z-1964-2018 - Maximal Barrier Drape; Product Codes: ASK-00002-1A | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Z-1965-2018 - Maximal Barrier Drape; Product Codes: ASK-00376-SU | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
| Z-1966-2018 - Maximal Barrier Drape; Product Code: ASK-01000-UPMS | 2 | 05/30/2018 |
FEI # 3015859709 Arrow International Inc |
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