Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K101572 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)- US. Siemens Material Numb... | 2 | 12/15/2022 | Siemens Healthcare Diagnostics, Inc. |
| IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS, except Japan Siemens Materi... | 2 | 12/15/2022 | Siemens Healthcare Diagnostics, Inc. |
| IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan Siemens Material Number (S... | 2 | 12/15/2022 | Siemens Healthcare Diagnostics, Inc. |
| 3gAllergy Specific IgE Universal Kit; Kit Component: 3gAllergy Specific IgE Adjustor Antibody (L2UN... | 2 | 11/13/2025 | Siemens Healthcare Diagnostics, Inc. |
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