XP-CR Tibial Tray - Interlok 69mm Item # 195272

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Number 562270 579210 663600 262410 445380 584280 590680 660460 663580 190400 190450 190460 190480 190470 190440 190490 190420 663620 996080 663620R 579230 043870 043880 090200 159240 090200R 159250 258070 283160 995970 206830 966730 374790 383690 283150 283150R 590690 352830 429250 322040 469500 456760 041290 827550 827540 585560 041220 503500 076030 221160 374060 221150 279020 712560 576010 672540 374050 821300 943380 450340 599130 600780 717170 017990 111580 111570 821290 220050 289180 121130 202930 218640 199730 351300 395430 395450 439670 445390 486110 351300R 395450R 439670R
  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 Biomet, Inc.
Reason for Recall:
The locking bar not fully engaging
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

XP-CR Tibial Tray - Interlok 69mm Item # 195272

Product Codes/Lot Numbers:

Lot Number 562270 579210 663600 262410 445380 584280 590680 660460 663580 190400 190450 190460 190480 190470 190440 190490 190420 663620 996080 663620R 579230 043870 043880 090200 159240 090200R 159250 258070 283160 995970 206830 966730 374790 383690 283150 283150R 590690 352830 429250 322040 469500 456760 041290 827550 827540 585560 041220 503500 076030 221160 374060 221150 279020 712560 576010 672540 374050 821300 943380 450340 599130 600780 717170 017990 111580 111570 821290 220050 289180 121130 202930 218640 199730 351300 395430 395450 439670 445390 486110 351300R 395450R 439670R

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2507-2019

Related Recalls

Zimmer Biomet is conducting a medical device correction to update the Instructions for Use (IFU) and the Surgical Techniques for the Polaris Spinal System Translation Screw and Cypher MIS Screw System. Users should be aware that changes were made to the contraindications section indicating that the Translation Screws should not be used with a direct current stimulation, as a high probability of construct failure exists when using Translation Screws containing CoCr with direct current simulation system.

Nov 17, 2020 Other Medical Devices Nationwide View Details →