FDA Adverse Event Injury Summary report: N

REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 7

MDR report key: 2677515 · Received July 27, 2012

Report

Report Number
2249697-2012-01014
Event Type
Injury
Date Received
July 27, 2012
Date of Event
July 9, 2012
Report Date
July 9, 2012
Manufacturer
STRYKER ORTHOPAEDICS MAHWAH
Product Code
MEH
PMA / PMN Number
K092561
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE FOLLOWING OTHER HIP DEVICES WERE ALSO LISTED IN THIS REPORT: LRG TAP PRI MOD NCK 8DEG 30MM, CAT# NLV-300800G, LOT# 31617901. TRIDENT PSL HA CLUSTER 54MM, CAT# 542-11-54F, LOT# MJELM8. TRIDENT 0 DEG INSERT 40MM, CAT# 623-00-40F, LOT# MJHPKJ. UNI ADAPTOR SLEEVE V40 TI, CAT# 6519-T-100, LOT# 3463081. DELTA UN FEM HD 40MM, CAT# 6519-1-040, LOT# 33669601. IT CANNOT BE DETERMINED WHICH, IF ANY OF THESE DEVICES MAY HAVE CAUSED OR CONTRIBUTED TO THE PT'S PAIN. AN EVAL OF THE DEVICE CANNOT BE PERFORMED AS THE DEVICE REMAINED IMPLANTED IN THE PT AND WAS NOT RETURNED TO THE MFR. ADD'L INFO (INCLUDING X-RAYS AND MEDICAL RECORDS) WAS REQUESTED. SHOULD ADD'L INFO BECOME AVAILABLE, THE EVAL SUMMARY WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.

Description of Event or Problem · 1

IT WAS REPORTED THAT, PT HAD ONSET OF HIP PAIN ON (B)(6) 2010.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 7 IMPLANT MEH STRYKER ORTHOPAEDICS MAHWAH NA MJD15L

Patients

Seq Age Sex Outcome Treatment
1 62 YR Other