Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
Class I - DangerousWhat Should You Do?
- Check if you have this product: model no. ME020R
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Aesculap, Inc.
- Reason for Recall:
- The trial insertion instrument may disassemble during use due to a potentially weak weld on then trial inserter shaft block area located near the thumb wheel.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
Product Codes/Lot Numbers:
model no. ME020R
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0361-2014
Related Recalls
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It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class I - Dangerous
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
Class I - Dangerous
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.