Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K120615 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Abbott Cholestech LDX Battery Kit, Model: 3LP656194-PCM-LD, PN: 55170 | 2 | 04/30/2024 | Alere San Diego, Inc. |
| The Cholestech LDX® System combines enzymatic methodology and solidphase technology to measure tota... | 2 | 08/06/2022 | Alere San Diego, Inc. |
| Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes o... | 2 | 09/05/2019 | Alere San Diego, Inc. |
| LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Cassette in box with foam inse... | 3 | 09/10/2016 | Alere San Diego, Inc. |
| Product Brand Name(s): Alere Cholestech LDX® Lipid Profile"GLU Test Cassette, Model 10-991. Product... | 3 | 11/22/2013 | Alere San Diego, Inc. |
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