Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K201887 |
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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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| Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor | 3 | 02/12/2026 |
FEI # 3018685978 SUREPULSE MEDICAL LTD |
| Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor | 3 | 02/12/2026 |
FEI # 3018685978 SUREPULSE MEDICAL LTD |
| Surepulse VS Cap Large REF: SP-162-A1 component of VS Newborn Heart Rate Monitor | 3 | 02/12/2026 |
FEI # 3018685978 SUREPULSE MEDICAL LTD |
| Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor | 3 | 02/12/2026 |
FEI # 3018685978 SUREPULSE MEDICAL LTD |
| Surepulse VS Cap Extra Large REF: SP-163-A1 component of VS Newborn Heart Rate Monitor | 3 | 02/12/2026 |
FEI # 3018685978 SUREPULSE MEDICAL LTD |
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