Medical Device Recalls
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41 to 50 of 500 Results
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow P... | 3 | 11/13/2025 |
FEI # 2250033 Accriva Diagnostics, Inc. |
| One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 30g 06949517008854 28g 06949... | 3 | 10/21/2025 |
FEI # 3021186226 Home Health US, Incorporated |
| FloPatch FP120, REF: FP120-FOT01-005 | 3 | 09/04/2025 |
FEI # 3015139886 Flosonics Medical (R/A 1929803 ONTARIO CORP.) |
| Akreos, SKU: AO60P0300. Akreos intraocular lenses | 3 | 08/26/2025 |
FEI # 1119279 Bausch & Lomb Surgical, Inc. |
| BP10-5ec Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| C10-3v Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| C10-4ec Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| c5-1 Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| C5-2 Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| C5-2 Lumify Transducer Probe | 3 | 08/22/2025 |
FEI # 2518586 Philips Ultrasound, Inc |
| * The maximium 500 devices meeting your search criteria returned. Please narrow your search. |
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