Ethicon Endo-Surgery Inc Endopath Probe Plus II, Hand-Controlled PistolGrip Handle, Product Code EPH02. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Endopath Probe Plus II, Hand-Controlled PistolGrip Handle, Product Code EPH02.
Brand
Ethicon Endo-Surgery Inc
Lot Codes / Batch Numbers
Lot C4DG7H and C4DL5W.
Products Sold
Lot C4DG7H and C4DL5W.
Ethicon Endo-Surgery Inc is recalling Endopath Probe Plus II, Hand-Controlled PistolGrip Handle, Product Code EPH02. due to There is the possibility of a seal void in the Probe Plus packaging which may have compromised the sterility of the device.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is the possibility of a seal void in the Probe Plus packaging which may have compromised the sterility of the device.
Recommended Action
Per FDA guidance
The recalling firm sent a recall letter by United Parcel Services to all consignees for delivery to each consignee on 4/24/06. The letter requested subaccount address return information to the recalling firm.
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