Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K141156 |
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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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| Xhibit Telemetry Receiver with Software, Model 96280. Intended to provide monitoring system with pa... | 2 | 01/07/2025 |
FEI # 3010157426 Spacelabs Healthcare, Inc. |
| Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system... | 2 | 01/07/2025 |
FEI # 3010157426 Spacelabs Healthcare, Inc. |
| Xhibit Telemetry Receiver, Model: 96280 | 2 | 08/11/2022 |
FEI # 3010157426 Spacelabs Healthcare, Inc. |
| Spacelabs Healthcare Xhibit Telemetry Receiver, Model 96280, software version 1.1, physiological pat... | 2 | 01/25/2018 |
FEI # 3010157426 Spacelabs Healthcare Inc |
| Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280. Xhibit Telemetry Receivers (XTR)... | 2 | 09/26/2016 |
FEI # 3010157426 Spacelabs Healthcare Inc |
| The Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280 is used to transmit patient(s)... | 2 | 08/22/2016 |
FEI # 3010157426 Spacelabs Healthcare Inc |
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