🔍 RecallPedia

Product 29 consists of all product under product code: LPHand same usage: Item no: 32902603800 FEMORAL HEAD +0.5 X 22 MM 32902604810 FEMORAL HEAD +3.5 X 22 MM 32902604845 FEMORAL HEAD +7.0 X 22 MM For use in total or hemi hip arthroplasty

Class I - Dangerous
🏥 Medical Devices Recalled: January 11, 2016 Zimmer Manufacturing B.V. Implants & Prosthetics Nationwide

What Should You Do?

  1. Check if you have this product:
    lot no.: 62051735 62221046 62262799 62272099 62279770 62279770N 62079181 62162466 62185965 62185966 62221047 62262801 62262802 62262803 62279771 62285361 62311660 62393063 62279771N 62285361N 62311660N 61520812 62162464 62221048 62279772 62393064 62279772N 62393064V
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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:
Zimmer Manufacturing B.V.
Reason for Recall:
As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Product 29 consists of all product under product code: LPHand same usage: Item no: 32902603800 FEMORAL HEAD +0.5 X 22 MM 32902604810 FEMORAL HEAD +3.5 X 22 MM 32902604845 FEMORAL HEAD +7.0 X 22 MM For use in total or hemi hip arthroplasty

Product Codes/Lot Numbers:

lot no.: 62051735 62221046 62262799 62272099 62279770 62279770N 62079181 62162466 62185965 62185966 62221047 62262801 62262802 62262803 62279771 62285361 62311660 62393063 62279771N 62285361N 62311660N 61520812 62162464 62221048 62279772 62393064 62279772N 62393064V

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1127-2016

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