MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US PINN 100 W/GRIPTION 56MM; PINNACLE HIP SYSTEM : HIP METAL ACETABULAR CUPS

Model Number 1217-31-056

Device Problems Device Dislodged or Dislocated (2923); Naturally Worn (2988); Noise, Audible (3273)

Patient Problems Pain (1994); Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)

Event Date 01/01/2021

Event Type  Injury  

Manufacturer Narrative

(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

Post tha the patient came back with a dissociated pinnacle poly liner leading to x-ray and will be revised.There was not a depuy head , they have put in a hybrid version with a stem and head from z/b.Due to the metal debris in the joint the or time was longer than expected.Approximately 30-45 minutes to clean out the metal debris from the tissues in the joint.There was a lot of metal debris in the hip joint witch was removed and a new altrx liner was implanted.The pinnacle cup-121731056 lot nr 9660625 was a bit worn on the edge but mostly the debris came from the metal head from z/b that also was exchanged.The head and stem is from z/b.The patient is a male and the affected side is right.

Manufacturer Narrative

Product complaint # (b)(4).Investigation summary : no device associated with this report was received for examination.Visual examination of the provided x-ray image confirmed the reported disassociation.A worldwide complaint database search found no other related reported incidents against the provided product code/lot number combination since release for distribution.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Device history lot : the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).Where the lot code was provided, a manufacturing records evaluation (mre) was not performed.

• Brand Name: PINN 100 W/GRIPTION 56MM
• Type of Device: PINNACLE HIP SYSTEM : HIP METAL ACETABULAR CUPS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 11590686
• MDR Text Key: 242998331
• Report Number: 1818910-2021-06491
• Device Sequence Number: 1
• Product Code: KWA
• UDI-Device Identifier: 10603295010227
• UDI-Public: 10603295010227
• Combination Product (y/n): N
• PMA/PMN Number: K090998
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Type of Report: Initial,Followup
• Report Date: 03/12/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/30/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 1217-31-056
• Device Catalogue Number: 121731056
• Device Lot Number: 9660625
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 05/12/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Treatment: PINN 100 W/GRIPTION 56MM; PINN MAR NEUT 32IDX56OD; UNKNOWN HIP FEMORAL HEAD; PINN 100 W/GRIPTION 56MM; PINN MAR NEUT 32IDX56OD; UNKNOWN HIP FEMORAL HEAD
• Patient Outcome(s): Required Intervention