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Welch Allyn, Inc.
WELCH ALLYN, INC. · Model 901141 · UDI-DI 00732094309294
10
510(k) clearances
63
Adverse events (1 deaths)
5
Recalls
50
Facilities
Description
Reconditioned H12+ 12-lead digital Holter Recorder - 24-hour with HF (high fidelity) for 24-hour high-fidelity recordings, includes HF compact flash card (1 GB), carry case, and hookup kit; Multiple languages and CD manual (except Brazilian Portuguese); IEC 10-wire, 12- lead LeadForm 38" (97cm) patient cable with snap ends
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-11-25 | Spacelabs Healthcare, Ltd. | Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder. The physical serial number label on the device might not match |
| 2024-11-25 | Spacelabs Healthcare, Ltd. | Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder. The physical serial number label on the device might not match |
| 2020-01-22 | Braemar Manufacturing, LLC | An issue with the DL900 and DL950 Series Holter Recorder was recognized on January 1, 2020. This issue can prevent the recorder from operating normally. Braemar confirmed that be |
| 2020-01-22 | Braemar Manufacturing, LLC | An issue with the DL900 and DL950 Series Holter Recorder was recognized on January 1, 2020. This issue can prevent the recorder from operating normally. Braemar confirmed that be |
| 2020-01-13 | Philips North America, LLC | if an AAA battery is inserted in the recorder and a user attempts to start it, or if the recorder is inserted in the docking station, the recorder will display Error: 602 and fai |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.