Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2041C-3254
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot Number: 53778501 UDIs: (01)04546540035806(17)201108(10)53778501
- 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:
- Howmedica Osteonics Corp.
- Reason for Recall:
- May have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2041C-3254
Product Codes/Lot Numbers:
Lot Number: 53778501 UDIs: (01)04546540035806(17)201108(10)53778501
Distribution:
Distributed in: CA, FL, GA, IA, MA, MI, NC, OH, WI
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0811-2020
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