Fukuda Denshi recalls
Fukuda Denshi appears in 1 official U.S. recall notice indexed by RecallRadar, most recently on 2017-12-13.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 1 |
|---|---|
| Published | 2017-12-13 |
| By agency | FDA Device (1) |
| By classification | Class II (1) |
| By status | completed (1) |
| Distribution named in notices | US |
Recalls
- Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage: Use of the Fukuda Denshi DynaScope Model DS-8100N/8100M Patient Mo…
FDA Device · Class II · 2017-12-13 · Fukuda Denshi
Reason: For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003% (17) of the 6227 devices sold worldwide, a Short-term Battery Error message has appeared and has been traced back to a bad (damaged) Lithium-Ion c…