Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055

Class I - Dangerous
🏥 Medical Devices Recalled: September 4, 2020 Biomet Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Numbers: 866270A 887060B 919100B 938510A 942310A 905460A 907080A 930110A 866270B 887070A 919110A 938510B 942310B 905460B 907080B 930110B 866280A 887070B 919110B 938520A 942320A 905470A 907090A 930120A 866280B 887080A 919120A 938520B 942320B 905470B 907090B 930120B 866290A 887080B 919120B 938530A 942330A 905480A 907100A 930130A 866290B 887090A 919130A 938530B 942330B 905480B 907100B 930130B 866300A 887090B 919130B 938540A 942340B 905490A 907110A 930140A 866300B 887100A 920410A 938540B 946900A 905490B 907110B 930140B 866310A 887100B 920410B 942150A 946900B 905500A 907120A 934570A 866310B 902920A 920420A 942150B 946910A 905500B 907120B 934570B 866320A 902920B 920420B 942160A 946910B 905520A 907130A 934580A 866320B 902930A 920430A 942160B 946930B 905520B 926660A 934580B 866330A 907130B 920430B 942180A 946940A 905530A 926660B 934590A 866330B 915230A 920440A 942180B 946950B 905530B 926670A 934590B 876100A 915230B 920440B 942190A 946960A 905540A 926670B 934600A 876100B 915240A 920450A 942190B 946960B 905540B 926680A 934600B 876110A 915240B 920450B 942200A 946980B 905550A 926680B 934610A 876110B 915250A 920460A 942200B 947010B 905550B 926690A 934610B 876120A 915250B 920460B 942210A 947020A 905560A 926690B 936120A 876120B 915260A 922170A 942210B 947020B 905560B 926700A 936120B 876130A 915260B 922170B 942220A 947030A 905640A 926700B 936130A 876130B 915270A 922180A 942220B 947030B 905640B 926710A 936130B 876140A 915270B 922180B 942230A 947040A 905650A 926710B 936140A 876140B 915280A 922190A 942230B 947040B 905650B 926720A 936140B 876150A 915280B 922190B 942240A 902930B 905660A 926720B 936150A 876150B 917710A 922200A 942240B 902940A 905660B 928920A 936150B 876160A 917710B 922200B 942250A 902940B 905670A 928920B 936160A 876160B 917720A 922210A 942250B 902950B 905670B 928930A 936160B 887010A 917720B 922210B 942260A 902960A 905680A 928930B 936170A 887010B 917730A 922220A 942260B 902960B 905680B 928940A 936170B 887020A 917730B 922220B 942270A 902970A 907040A 928940B 936180A 887020B 917740A 922230A 942270B 902970B 907040B 928950A 936180B 887030A 917740B 922230B 942280A 902980A 907050A 928950B 936190A 887030B 917750A 922240A 942280B 902980B 907050B 928960A 936190B 887040A 917750B 922240B 942290A 902990A 907060A 928960B 938490A 887040B 919090A 926650A 942290B 903000A 907060B 930100A 938490B 887050A 919090B 926650B 942300A 903010A 907070A 930100B 938500A 887050B 919100A 938500B 942300B 903010B 907070B
  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:
Biomet, Inc.
Reason for Recall:
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055

Product Codes/Lot Numbers:

Lot Numbers: 866270A 887060B 919100B 938510A 942310A 905460A 907080A 930110A 866270B 887070A 919110A 938510B 942310B 905460B 907080B 930110B 866280A 887070B 919110B 938520A 942320A 905470A 907090A 930120A 866280B 887080A 919120A 938520B 942320B 905470B 907090B 930120B 866290A 887080B 919120B 938530A 942330A 905480A 907100A 930130A 866290B 887090A 919130A 938530B 942330B 905480B 907100B 930130B 866300A 887090B 919130B 938540A 942340B 905490A 907110A 930140A 866300B 887100A 920410A 938540B 946900A 905490B 907110B 930140B 866310A 887100B 920410B 942150A 946900B 905500A 907120A 934570A 866310B 902920A 920420A 942150B 946910A 905500B 907120B 934570B 866320A 902920B 920420B 942160A 946910B 905520A 907130A 934580A 866320B 902930A 920430A 942160B 946930B 905520B 926660A 934580B 866330A 907130B 920430B 942180A 946940A 905530A 926660B 934590A 866330B 915230A 920440A 942180B 946950B 905530B 926670A 934590B 876100A 915230B 920440B 942190A 946960A 905540A 926670B 934600A 876100B 915240A 920450A 942190B 946960B 905540B 926680A 934600B 876110A 915240B 920450B 942200A 946980B 905550A 926680B 934610A 876110B 915250A 920460A 942200B 947010B 905550B 926690A 934610B 876120A 915250B 920460B 942210A 947020A 905560A 926690B 936120A 876120B 915260A 922170A 942210B 947020B 905560B 926700A 936120B 876130A 915260B 922170B 942220A 947030A 905640A 926700B 936130A 876130B 915270A 922180A 942220B 947030B 905640B 926710A 936130B 876140A 915270B 922180B 942230A 947040A 905650A 926710B 936140A 876140B 915280A 922190A 942230B 947040B 905650B 926720A 936140B 876150A 915280B 922190B 942240A 902930B 905660A 926720B 936150A 876150B 917710A 922200A 942240B 902940A 905660B 928920A 936150B 876160A 917710B 922200B 942250A 902940B 905670A 928920B 936160A 876160B 917720A 922210A 942250B 902950B 905670B 928930A 936160B 887010A 917720B 922210B 942260A 902960A 905680A 928930B 936170A 887010B 917730A 922220A 942260B 902960B 905680B 928940A 936170B 887020A 917730B 922220B 942270A 902970A 907040A 928940B 936180A 887020B 917740A 922230A 942270B 902970B 907040B 928950A 936180B 887030A 917740B 922230B 942280A 902980A 907050A 928950B 936190A 887030B 917750A 922240A 942280B 902980B 907050B 928960A 936190B 887040A 917750B 922240B 942290A 902990A 907060A 928960B 938490A 887040B 919090A 926650A 942290B 903000A 907060B 930100A 938490B 887050A 919090B 926650B 942300A 903010A 907070A 930100B 938500A 887050B 919100A 938500B 942300B 903010B 907070B

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0083-2021

Related Recalls