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-0064-2025 - Blue Diamond Digital Inflation Device, REF: IN7152/C, IN7352/C, IN7403/C, IN7802/C, IN7852/C, IN7130/C | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
| Z-0065-2025 - basixTOUCH Inflation Device, REF: IN8140/A | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
| Z-0066-2025 - DiamondTOUCH Digital Inflation Device, REF: IN9135/A, IN9152/A | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
| Z-0067-2025 - IntelliSystem Inflation Device, REF: IN1525/D | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
| Z-0073-2025 - StabiliT TOUCH Syringe, REF: IN8VCF/B | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
| Z-0069-2025 - MONARCH Inflation Device, REF: IN2430/B, IN2530/B, IN2130/B | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
| Z-0070-2025 - Custom Inflation Kit, REF: K05-00052M, K05-00053H, K05-00109G, K05-00137K, K05-00296L, K05-00399D, K05-00404C, K05-00410G, K05-00438G, K05-00502F, K05-00564L, K05-00587D, K05-00612Q, K05-00704F, K05-0... | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
| Z-0071-2025 - basixSKY Inflation Device, REF: SKY1802 | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
| Z-0072-2025 - basixTOUCH Inflation Device, REF: IN8130/JPC, IN8152/C, IN8302/C, IN8352/C, IN8802/C, IN8130/C, IN8130/C | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
| Z-0068-2025 - BlueFIRE Inflation Device, REF: IN10140 | 2 | 10/11/2024 |
FEI # 1721504 Merit Medical Systems, Inc. |
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