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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ETHICON INC. PHYSIOMESH UNKNOWN PRODUCT; MESH, SURGICAL
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ETHICON INC. PHYSIOMESH UNKNOWN PRODUCT; MESH, SURGICAL Back to Search Results
Catalog Number PHYSIOMUNK
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Injury (2348); Not Applicable (3189)
Event Type  Injury  
Manufacturer Narrative
(b)(4).To date, the device has not been returned.If the product is returned for evaluation, any further information derived from the evaluation will be submitted in a supplemental 3500a form.
 
Event Description
It was reported by an attorney that the patient underwent a hernia repair procedure on (b)(6) 2015 and mesh was implanted.It was reported the patient experienced an undisclosed adverse event.No additional information was provided.
 
Manufacturer Narrative
Date sent to fda: 2/28/2019.Additional narrative: it was reported that the patient underwent mesh removal surgery on (b)(6) 2017.In addition, a review of the manufacturing records was performed and indicates that there were no quality concerns associated with the manufacturing process.
 
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Brand Name
PHYSIOMESH UNKNOWN PRODUCT
Type of Device
MESH, SURGICAL
Manufacturer (Section D)
ETHICON INC.
p.o. box 151, route 22 west
somerville NJ 08876 0151
MDR Report Key8194573
MDR Text Key131370936
Report Number2210968-2018-77644
Device Sequence Number1
Product Code FTL
Combination Product (y/n)N
PMA/PMN Number
K093932
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type other
Type of Report Initial,Followup
Report Date 02/21/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/25/2018
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date03/31/2017
Device Catalogue NumberPHYSIOMUNK
Device Lot NumberJD8GCZB1
Was Device Available for Evaluation? No
Date Manufacturer Received02/21/2019
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
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