FEM PRC LT M/RT L SML FEM PRC RT M/LT L SML FEM PRC LT M/RT L SML+ FEM PRC RT M/LT L SML+ FEM PRC LT M/RT L REG FEM PRC RT M/LT L REG FEM PRC LT M/RT L REG+ FEM PRC RT M/LT L REG+ FEM PRC LT M/RT L LGE FEM PRC RT M/LT L LGE FEM PRC LT M/RT L LGE+ FEM PRC RT M/LT L LGE+ " These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or function. - Varus or valgus deformities. - Revision of previous arthroplasty procedures. " These devices are indicated for cemented use only. " The Zimmer Unicompartmental Knee System is designed for use when load bearing ROM is expected to be less than or equal to 155 degrees.

Class I - Dangerous

🏥 Medical Devices Recalled: November 29, 2017 Zimmer Biomet Implants & Prosthetics Nationwide

What Should You Do?

Check if you have this product:
00-5790-020-00 00-5790-021-00 00-5790-022-00 00-5790-023-00 00-5790-024-00 00-5790-025-00 00-5790-026-00 00-5790-027-00 00-5790-028-00 00-5790-029-00 00-5790-030-00 00-5790-031-00 00-5790-020-00 61855504 00-5790-020-00 11004267 00-5790-020-00 61933229 00-5790-020-00 61915949 00-5790-020-00 11005144 00-5790-020-00 61949771 00-5790-020-00 62062057 00-5790-020-00 77001776 00-5790-022-00 61788933 00-5790-022-00 61810168 00-5790-022-00 61831670 00-5790-022-00 61894364 00-5790-022-00 11004689 00-5790-022-00 61910487 00-5790-022-00 61932359 00-5790-022-00 11004850 00-5790-022-00 61939861 00-5790-022-00 61958404 00-5790-022-00 61993535 00-5790-022-00 61987879 00-5790-022-00 62041075 00-5790-022-00 62074833 00-5790-022-00 11006797 00-5790-022-00 77001778 00-5790-024-00 61788934 00-5790-024-00 61805631 00-5790-024-00 61822278 00-5790-024-00 61928510 00-5790-024-00 61952565 00-5790-024-00 62025572 00-5790-024-00 62054459 00-5790-024-00 62068114 00-5790-024-00 62080645 00-5790-024-00 62105235 00-5790-024-00 77001780 00-5790-024-00 62110658 00-5790-026-00 61777601 00-5790-026-00 61815430 00-5790-026-00 61824552 00-5790-026-00 61952567 00-5790-026-00 62005615 00-5790-026-00 11006199 00-5790-026-00 62062058 00-5790-026-00 62086067 00-5790-026-00 77001782 00-5790-028-00 61831671 00-5790-028-00 62062059 00-5790-028-00 11006735 00-5790-028-00 77001784 00-5790-030-00 61881087 00-5790-030-00 61968455 00-5790-030-00 77001786 00-5790-021-00 61933230 00-5790-021-00 11005163 00-5790-021-00 11005243 00-5790-021-00 62013359 00-5790-021-00 11006254 00-5790-021-00 62086803 00-5790-021-00 77001777 00-5790-023-00 11003416 00-5790-023-00 61795864 00-5790-023-00 11003680 00-5790-023-00 61810169 00-5790-023-00 11003843 00-5790-023-00 61889207 00-5790-023-00 61904081 00-5790-023-00 61933231 00-5790-023-00 61928509 00-5790-023-00 61949247 00-5790-023-00 61993546 00-5790-023-00 62020300 00-5790-023-00 62056497 00-5790-023-00 62074834 00-5790-023-00 77001779 00-5790-025-00 61777599 00-5790-025-00 61795865 00-5790-025-00 61822279 00-5790-025-00 61899451 00-5790-025-00 61928511 00-5790-025-00 61936678 00-5790-025-00 61952566 00-5790-025-00 11005169 00-5790-025-00 62000808 00-5790-025-00 62020301 00-5790-025-00 62056498 00-5790-025-00 62074835 00-5790-025-00 62080646 00-5790-025-00 11006839 00-5790-025-00 62104129 00-5790-025-00 77001781 00-5790-027-00 61782626 00-5790-027-00 61824553 00-5790-027-00 61921258 00-5790-027-00 61952568 00-5790-027-00 62045723 00-5790-027-00 62068115 00-5790-027-00 62092386 00-5790-027-00 77001783 00-5790-029-00 61805632 00-5790-029-00 62005616 00-5790-029-00 77001785 00-5790-031-00 62002487 00-5790-031-00 77001787
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:: Zimmer Biomet, Inc.
Reason for Recall:: The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: terminated

Product Information

Full Description:

FEM PRC LT M/RT L SML FEM PRC RT M/LT L SML FEM PRC LT M/RT L SML+ FEM PRC RT M/LT L SML+ FEM PRC LT M/RT L REG FEM PRC RT M/LT L REG FEM PRC LT M/RT L REG+ FEM PRC RT M/LT L REG+ FEM PRC LT M/RT L LGE FEM PRC RT M/LT L LGE FEM PRC LT M/RT L LGE+ FEM PRC RT M/LT L LGE+ " These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or function. - Varus or valgus deformities. - Revision of previous arthroplasty procedures. " These devices are indicated for cemented use only. " The Zimmer Unicompartmental Knee System is designed for use when load bearing ROM is expected to be less than or equal to 155 degrees.

Product Codes/Lot Numbers:

00-5790-020-00 00-5790-021-00 00-5790-022-00 00-5790-023-00 00-5790-024-00 00-5790-025-00 00-5790-026-00 00-5790-027-00 00-5790-028-00 00-5790-029-00 00-5790-030-00 00-5790-031-00 00-5790-020-00 61855504 00-5790-020-00 11004267 00-5790-020-00 61933229 00-5790-020-00 61915949 00-5790-020-00 11005144 00-5790-020-00 61949771 00-5790-020-00 62062057 00-5790-020-00 77001776 00-5790-022-00 61788933 00-5790-022-00 61810168 00-5790-022-00 61831670 00-5790-022-00 61894364 00-5790-022-00 11004689 00-5790-022-00 61910487 00-5790-022-00 61932359 00-5790-022-00 11004850 00-5790-022-00 61939861 00-5790-022-00 61958404 00-5790-022-00 61993535 00-5790-022-00 61987879 00-5790-022-00 62041075 00-5790-022-00 62074833 00-5790-022-00 11006797 00-5790-022-00 77001778 00-5790-024-00 61788934 00-5790-024-00 61805631 00-5790-024-00 61822278 00-5790-024-00 61928510 00-5790-024-00 61952565 00-5790-024-00 62025572 00-5790-024-00 62054459 00-5790-024-00 62068114 00-5790-024-00 62080645 00-5790-024-00 62105235 00-5790-024-00 77001780 00-5790-024-00 62110658 00-5790-026-00 61777601 00-5790-026-00 61815430 00-5790-026-00 61824552 00-5790-026-00 61952567 00-5790-026-00 62005615 00-5790-026-00 11006199 00-5790-026-00 62062058 00-5790-026-00 62086067 00-5790-026-00 77001782 00-5790-028-00 61831671 00-5790-028-00 62062059 00-5790-028-00 11006735 00-5790-028-00 77001784 00-5790-030-00 61881087 00-5790-030-00 61968455 00-5790-030-00 77001786 00-5790-021-00 61933230 00-5790-021-00 11005163 00-5790-021-00 11005243 00-5790-021-00 62013359 00-5790-021-00 11006254 00-5790-021-00 62086803 00-5790-021-00 77001777 00-5790-023-00 11003416 00-5790-023-00 61795864 00-5790-023-00 11003680 00-5790-023-00 61810169 00-5790-023-00 11003843 00-5790-023-00 61889207 00-5790-023-00 61904081 00-5790-023-00 61933231 00-5790-023-00 61928509 00-5790-023-00 61949247 00-5790-023-00 61993546 00-5790-023-00 62020300 00-5790-023-00 62056497 00-5790-023-00 62074834 00-5790-023-00 77001779 00-5790-025-00 61777599 00-5790-025-00 61795865 00-5790-025-00 61822279 00-5790-025-00 61899451 00-5790-025-00 61928511 00-5790-025-00 61936678 00-5790-025-00 61952566 00-5790-025-00 11005169 00-5790-025-00 62000808 00-5790-025-00 62020301 00-5790-025-00 62056498 00-5790-025-00 62074835 00-5790-025-00 62080646 00-5790-025-00 11006839 00-5790-025-00 62104129 00-5790-025-00 77001781 00-5790-027-00 61782626 00-5790-027-00 61824553 00-5790-027-00 61921258 00-5790-027-00 61952568 00-5790-027-00 62045723 00-5790-027-00 62068115 00-5790-027-00 62092386 00-5790-027-00 77001783 00-5790-029-00 61805632 00-5790-029-00 62005616 00-5790-029-00 77001785 00-5790-031-00 62002487 00-5790-031-00 77001787

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1055-2018

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