ADVANTX LCLP+
Class I - DangerousWhat Should You Do?
- Check if you have this product: Mfg. Lot or Serial # System ID 00000047915YY4 415540ADVLCLP 00000063721YY5 909865LCLP Not Available 916734XR 00000063736YY3 MCTHKGMN 00000023830YY3 912633MCL1 00000023761YY0 912633MCL1 00000128484M03 312CCHGECATH 00000128484MO3 312CCHGECATH Not Available 507255CC101 Not Available LIJ015064 00000026160YY2 210428VCATH2 00000063805YY6 BPEP Not Available 414C4862 00000022150YY7 YX0738
- 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:
- GE Healthcare, LLC
- Reason for Recall:
- GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
ADVANTX LCLP+
Product Codes/Lot Numbers:
Mfg. Lot or Serial # System ID 00000047915YY4 415540ADVLCLP 00000063721YY5 909865LCLP Not Available 916734XR 00000063736YY3 MCTHKGMN 00000023830YY3 912633MCL1 00000023761YY0 912633MCL1 00000128484M03 312CCHGECATH 00000128484MO3 312CCHGECATH Not Available 507255CC101 Not Available LIJ015064 00000026160YY2 210428VCATH2 00000063805YY6 BPEP Not Available 414C4862 00000022150YY7 YX0738
Distribution:
Nationwide distribution
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0906-2017
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