Catalog Number 5700000000 |
Device Problems
Entrapment of Device (1212); False Reading From Device Non-Compliance (1228)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 02/13/2017 |
Event Type
malfunction
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Manufacturer Narrative
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Once the shipping pins were removed from the unit, the scale functioned properly.
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Event Description
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It was reported by service report that the scale was inaccurate due to shipping pins being left in the unit.No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
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Event Description
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It was reported by service report that the scale was inaccurate due to shipping pins being left in the unit.No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
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Search Alerts/Recalls
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