Zimmer Inc. M/DN Intramedullary Fixation Humeral Nail Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
M/DN Intramedullary Fixation Humeral Nail
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
Catalog no. 00-2254-195-09 Lot # 20118000
Products Sold
Catalog no. 00-2254-195-09 Lot # 20118000
Zimmer Inc. is recalling M/DN Intramedullary Fixation Humeral Nail due to One and possibly more units in the lot have the proximal angled hole oriented 180 degrees reversed from the required orientation.. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: distribution information.
Reason for Recall
As stated by FDA
One and possibly more units in the lot have the proximal angled hole oriented 180 degrees reversed from the required orientation.
Recommended Action
Per FDA guidance
Units were distributed to twelve (12) consignees in the US and seven (7) foreign consignees (China, Japan, Korea, El Salvador, Singapore, Taiwan and UK)
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