Nihon Kohden recalls expired Adult Cap-ONE Biteblock models YG-227T due to distribution after expiration. These devices may not function safely during endoscopy procedures.
Due to products being shipped/distributed to customers after the products expiration date had past.
Nihon Kohden is recalling adult Cap-ONE Biteblocks with model YG-227T that were shipped after their expiration date. Using expired medical devices could lead to unsafe oxygen administration during endoscopy procedures.
The devices were distributed after their expiration date, which could mean they no longer function properly. Expired medical devices may not deliver oxygen safely during endoscopy procedures.
Patients undergoing endoscopy procedures who use the recalled Cap-ONE Biteblocks. Those with the specific model numbers 706121CB, 706301CB, or 707211CB are most at risk.
Check for model number YG-227T on the device. Look for lot numbers 706121CB, 706301CB, or 707211CB on the packaging or label.
Verify the device's expiration date and lot number to confirm if it's in the recalled range.
The products were shipped and distributed after their expiration date, which could affect their safety during endoscopy procedures.
Model YG-227T with lot numbers 706121CB, 706301CB, and 707211CB.
The recall does not require immediate stop use; check expiration and lot numbers to determine if it's affected.
We’ve drafted a message you can send Nihon Koh: The record says 'Nihon Kohden America Inc' — so the brand display is 'Nihon Kohden' (shortened from the legal name, common in consumer contexts). to request your refund or repair — edit it as you like.
Subject: Recall Z-0314-2025 — Nihon Koh: The record says 'Nihon Kohden America Inc' — so the brand display is 'Nihon Kohden' (sho Hello, I own a Nihon Koh: The record says 'Nihon Kohden America Inc' — so the brand display is 'Nihon Kohden' (shortened from the legal name, common in consumer contexts). that is covered by recall Z-0314-2025 from Nihon Koh: The record says 'Nihon Kohden America Inc' — so the brand display is 'Nihon Kohden' (shortened from the legal name, common in consumer contexts).. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
