FDA Adverse Event Injury Summary report: N

UNK HIP ACETABULAR CUP PINNACLE

MDR report key: 14931168 · Received July 6, 2022

Report

Report Number
1818910-2022-12376
Event Type
Injury
Date Received
July 6, 2022
Date of Event
January 11, 2022
Report Date
July 6, 2022
Manufacturer
DEPUY ORTHOPAEDICS INC US
Product Code
LPH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

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.

Additional Manufacturer Narrative · 0

PRODUCT COMPLAINT # (B)(4). INVESTIGATION SUMMARY ==> NO DEVICE ASSOCIATED WITH THIS REPORT WAS RECEIVED FOR EXAMINATION. THIS COMPLAINT WAS OPENED TO DOCUMENT COMPLAINTS DERIVED THROUGH A JOURNAL ARTICLE REVIEW. FOLLOW-UPS WERE DONE TO TRY AND OBTAIN ADDITIONAL INFORMATION FROM THE AUTHOR OF THE JOURNAL ARTICLE. NO FURTHER INFORMATION WAS RECEIVED. DEVICE HISTORY LOT ==> A MANUFACTURING RECORD EVALUATION (MRE), WAS NOT POSSIBLE BECAUSE THE REQUIRED LOT CODE WAS NOT PROVIDED.

Description of Event or Problem · 0

THIS COMPLAINT IS FROM A LITERATURE SOURCE. THE FOLLOWING LITERATURE CITE HAS BEEN REVIEWED KOBAYASHI K, OSAKI M, KIDERA K, AIT-SI-SELMI T, RAMOS-PASCUAL S, SAFFARINI M, BONNIN MP. STEM-BONE CONTACT PATTERNS OF A LONG STRAIGHT TAPERED UNCEMENTED STEM FOR PRIMARY THA. ARCH ORTHOP TRAUMA SURG. 2022 JAN 11. DOI: 10.1007/S00402-021-04273-5. EPUB AHEAD OF PRINT. PMID: 35013767. OBJECTIVE AND METHODS: THIS STUDY AIMED TO INVESTIGATE STEM-BONE CONTACT PATTERNS OF A LONG STRAIGHT-TAPERED UNCEMENTED STEM FOLLOWING PRIMARY THA, AND TO DETERMINE WHETHER THESE CONTACT PATTERNS ARE RELATED TO PREOPERATIVE FEMORAL MORPHOLOGY AND WHETHER THEY INFLUENCE POSTOPERATIVE OUTCOMES. THE AUTHORS REVIEWED A CONTINUOUS SERIES OF 60 HIPS (55 PATIENTS) THAT UNDERWENT PRIMARY THA USING THE CORAIL/PINNACLE DEVICES (DEPUY, LEEDS, UK). THE ACETABULAR LINER AND FEMORAL HEADS ARE NOT SPECIFIED BUT ASSUMED TO BE DEPUY PRODUCTS. PATIENTS WERE EVALUATED PRE- AND POST-OPERATIVELY USING THE JAPANESE ORTHOPAEDIC ASSOCIATION (JOA) SCORE. THE AUTHORS CONCLUDED THAT THE STEM-BONE CONTACT PATTERNS OF A LONG STRAIGHT-TAPERED UNCEMENTED STEM ARE RELATED TO PREOPERATIVE FEMORAL MORPHOLOGY, BUT DO NOT INFLUENCE SHORT-TERM POSTOPERATIVE OUTCOMES. LOT, MODEL AND CATALOG NUMBER ARE NOT AVAILABLE, BUT THE SUSPECTED DEPUY DEVICE POSSIBLY ASSOCIATED WITH REPORTED ADVERSE EVENTS: PINNACLE CUP, CORAIL STEM, UNKNOWN HEAD AND LINER. ADVERSE EVENT(S) AND PROVIDED INTERVENTIONS ASSOCIATED WITH DEPUY DEVICES: 1 REPORT OF RECURRENT DISLOCATION ATTRIBUTED TO A MALPOSITIONED CUP. TREATMENT WAS A CLOSED REDUCTION AND 3 MONTHS IN AN UNSPECIFIED PROTECTIVE HIP BRACE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1620281 UNK HIP ACETABULAR CUP PINNACLE HIP ACETABULAR CUP LPH DEPUY ORTHOPAEDICS INC US

Patients

Seq Age Sex Outcome Treatment
1 Unknown Required Intervention UNK HIP ACETABULAR CUP PINNACLE| UNKNOWN HIP ACETABULAR LINERS| UNKNOWN HIP FEMORAL HEAD