EVERA MRI S DR SureScan, Model Number DDMC3D4, Implantable Cardioverter Defibrillator
Class I - DangerousWhat Should You Do?
- Check if you have this product: GTIN: 00763000206185, Serial Numbers: PHZ659606S, PHZ659607S, PHZ659610S, PHZ659611S, PHZ659612S, PHZ659666S, PHZ659667S, PHZ659693S, PHZ659694S, PHZ659696S, PHZ659707S, PHZ659729S, PHZ659745S, PHZ659749S, PHZ659750S, PHZ659753S, PHZ659754S, PHZ659755S, PHZ659803S, PHZ659804S, PHZ659805S, PHZ659806S, PHZ659807S, PHZ659884S, PHZ659886S, PHZ659890S, PHZ659892S, PHZ659907S, PHZ659908S, PHZ659996S, PHZ660020S; GTIN: 00763000612023, Serial Numbers: PHZ659058S, PHZ659064S, PHZ659065S, PHZ659066S, PHZ659069S, PHZ659075S, PHZ659077S, PHZ659078S; GTIN: 00763000740443, Serial Number: PHZ659565S.
- 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:
- Medtronic Inc.
- Reason for Recall:
- Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
EVERA MRI S DR SureScan, Model Number DDMC3D4, Implantable Cardioverter Defibrillator
Product Codes/Lot Numbers:
GTIN: 00763000206185, Serial Numbers: PHZ659606S, PHZ659607S, PHZ659610S, PHZ659611S, PHZ659612S, PHZ659666S, PHZ659667S, PHZ659693S, PHZ659694S, PHZ659696S, PHZ659707S, PHZ659729S, PHZ659745S, PHZ659749S, PHZ659750S, PHZ659753S, PHZ659754S, PHZ659755S, PHZ659803S, PHZ659804S, PHZ659805S, PHZ659806S, PHZ659807S, PHZ659884S, PHZ659886S, PHZ659890S, PHZ659892S, PHZ659907S, PHZ659908S, PHZ659996S, PHZ660020S; GTIN: 00763000612023, Serial Numbers: PHZ659058S, PHZ659064S, PHZ659065S, PHZ659066S, PHZ659069S, PHZ659075S, PHZ659077S, PHZ659078S; GTIN: 00763000740443, Serial Number: PHZ659565S.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2199-2024
Related Recalls
There is a potential for delayed time to high-voltage (HV) therapy should a rare sequence of events occur.
In prior SmartSync application versions, the Abort button stopped the test that was selected. During an induction test, there was a limited window of time for the user to abort a therapy, thereby limiting the user's ability to cancel a high voltage therapy delivery.
In prior SmartSync application versions, the Abort button stopped the test that was selected. During an induction test, there was a limited window of time for the user to abort a therapy, thereby limiting the user's ability to cancel a high voltage therapy delivery.