Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K161313 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch di... | 2 | 10/19/2022 |
FEI # 3013162291 ARROW INTERNATIONAL Inc. |
| Arrowg+ard Blue Advance Midline Product Code: PR 41541 BAS | 2 | 06/16/2019 |
FEI # 3015859709 Arrow International Inc |
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