Zimmer, Inc. VER2 HANDLE, PIN REWORK, LT Nonsterile Recall
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VER2 HANDLE, PIN REWORK, LT Nonsterile
Brand
Zimmer, Inc.
Lot Codes / Batch Numbers
Item Number 82-0167-612-31, Lot Number 97009753, 97010150
Products Sold
Item Number 82-0167-612-31, Lot Number 97009753, 97010150
Zimmer, Inc. is recalling VER2 HANDLE, PIN REWORK, LT Nonsterile due to The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of . This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026