Medical Device Recalls
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31 to 36 of 36 Results
510(K) Number: K001245 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Cardiovascular Custom Procedure Kits, REV: 2A, REV: 2B X-COATED FX PK Item Number: 73191 Terumo ... | 2 | 09/16/2011 | Terumo Cardiovascular Systems Corp |
TruChoice Alliant Healthcare Products, REFERENCE# SSD-100EX, QUANTITY: 25, DESCRIPTION: TUBING W/ ON... | 2 | 08/23/2011 | Alliant Enterprises LLC |
Non-Adjustable Vent Valve, TruChoice Alliant Healthcare Products, REFERENCE#213-035 QUANTITY: 25, DE... | 2 | 08/23/2011 | Alliant Enterprises LLC |
Non-Adjustable Vent Valve, TruChoice Alliant Healthcare Products, REFERENCE#213-035NS QUANTITY: 100,... | 2 | 08/23/2011 | Alliant Enterprises LLC |
Adjustable Vent Valve, TruChoice Alliant Healthcare Products REFERENCE#213-030NS QUANTITY: 100 DESCR... | 2 | 08/23/2011 | Alliant Enterprises LLC |
Adjustable Vent Valve, TruChoice Alliant Healthcare Products REFERENCE#213-030 QUANTITY: 25 DESCRIPT... | 2 | 08/23/2011 | Alliant Enterprises LLC |
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