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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US QUICKSET ACE GRATER HEAD 45MM; HIP INSTRUMENTS : REAMERS

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DEPUY ORTHOPAEDICS INC US QUICKSET ACE GRATER HEAD 45MM; HIP INSTRUMENTS : REAMERS Back to Search Results
Catalog Number 244000545
Device Problems Dull, Blunt (2407); Failure to Cut (2587)
Patient Problem Not Applicable (3189)
Event Date 01/30/2020
Event Type  malfunction  
Manufacturer Narrative
Product complaint # (b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
 
Event Description
They have in consignment 9 stem instrument sets and 6 acetabular instr sets,as they have been waiting for 3 more new acetabular instr sets since (b)(6) 2019.In the meantime, we have left 2 sets of acetabular instruments from oc in order to cover those busy days.They opened those 2 loaners yesterday, and for both of them,the surgeons just could not do the reaming as they said the reamers were totally dull.They had to open zimmer acetabular instruments to finish their surgeries.
 
Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.Product complaint # (b)(4).Investigation summary: examination of the returned instrument confirmed the complaint.Depuy-synthes considers the investigation closed at this time.Should additional information be received, the information will be reviewed, and the investigation will be re-opened as necessary.Johnson & johnson canada reported that reamers are dull.Examination of the returned instrument confirmed the complaint of dullness.The complaint sample consisted of (1) quickset ace grater head 55mm, lot so2001192 a search of as400 indicated that this device was distributed for use on 27 oct 2011.A search of the complaint database found similar reports and the root cause is attributed to heavy use and wear out.Based on the investigation, the need for corrective action is not indicated.Complaints will be monitored under sep 419 post market surveillance.If information is obtained that was not available for the initial medwatch, a follow-up medwatch, a follow-up medwatch will be filed as appropriate.
 
Manufacturer Narrative
Product complaint (b)(4).Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.
 
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Brand Name
QUICKSET ACE GRATER HEAD 45MM
Type of Device
HIP INSTRUMENTS : REAMERS
Manufacturer (Section D)
DEPUY ORTHOPAEDICS INC US
700 orthopaedic drive
warsaw IN 46581 0988
MDR Report Key9729327
MDR Text Key190171670
Report Number1818910-2020-05356
Device Sequence Number1
Product Code HTO
UDI-Device Identifier10603295123927
UDI-Public10603295123927
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,foreig
Type of Report Initial,Followup,Followup
Report Date 03/24/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/19/2020
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Catalogue Number244000545
Device Lot NumberSO2001192
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer03/10/2020
Date Manufacturer Received03/24/2020
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
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