cap-ONE YG-227TRecalls & reported problems
Nihon Kohden Corporation · Adult Cap-ONE Biteblock · Class 1
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Apr 29, 2022Open, Classified
Due to products being shipped/distributed to customers after the products expiration date had past.
Z-0314-2025 · Root cause: Process control · FDA record ↗
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- Blox™ SBT-546Boston Scientific Corporation · Endoscopic bite block8 reports
- NA 00712804US Endoscopy · Endoscopic bite block3 reports
- Blox™ SBT-321Boston Scientific Corporation · Endoscopic bite block2 reports
- Mouthpiece MB-142Olympus Medical Systems Corp. · Endoscopic Bite Block1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.