Medical Devices
U & I America 4mm Hex Driver Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
4mm Hex Driver
Brand
U & I America
Lot Codes / Batch Numbers
Part Number MU20012, Revision I, Lot # 02190301, 05120311
Products Sold
Part Number MU20012, Revision I, Lot # 02190301, 05120311
U & I America is recalling 4mm Hex Driver due to Reports of hex driver tips breaking off or becoming worn or stripped.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reports of hex driver tips breaking off or becoming worn or stripped.
Recommended Action
Per FDA guidance
The only consignee was notified by letter on 1/14/2003.
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 noticeDistribution
As reported by FDA
MN
Page updated: Jan 10, 2026