Reported Oct 14, 2020 · Terminated
Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055
Biomet, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
- Biomet ONPOINT
- SCOPE PROCEDURE KIT-EU Item Number24-3055
- Lot codes and dates
- Lot Numbers
302 of 302 codes
866270A887060B919100B938510A942310A905460A907080A930110A866270B887070A919110A938510B942310B905460B907080B930110B866280A887070B919110B938520A942320A905470A907090A930120A866280B887080A919120A938520B942320B905470B907090B930120B866290A887080B919120B938530A942330A905480A907100A930130A866290B887090A919130A938530B942330B905480B907100B930130B866300A887090B919130B938540A942340B905490A907110A930140A866300B887100A920410A938540B
- Lot Numbers
- Amount recalled
- US: 33 units; OUS: 269 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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