MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US S-ROM*SLEEVE PRX ZTT, 14B-SML; S-ROM HIP SYSTEM : HIP FEMORAL SLEEVE

Model Number 55-0501

Device Problem Difficult to Remove (1528)

Patient Problems Bone Fracture(s) (1870); Not Applicable (3189); No Code Available (3191)

Event Date 12/26/2019

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

It was reported that crush fracture occurred during the revision surgery on (b)(6) 2019 (the revision surgery was reported once as (b)(4).The surgeon was planning to remain the stem (p/n: 900526210) with the sleeve (p/n: 550501) and performed head trial however dislocation occurred due to leg length mismatch.Therefore, the surgeon attempted to remain the sleeve and explant only the stem with a dedicated stem extractor for replacing the stem, but it could not be done.Originally, despite being implants that can be easily replaced, the stem and the sleeve were coming out together when s/he attempted to explant only the stem again.At the same time, a part of the proximal medial part of the femur and the greater trochanter were crushed fracture and bleeding heavily.Thus, a srom stem which was prepared for the patient could not use.Since the surgery could not continue due to crush fracture occurrence, the wound was closed, and the 2nd revision surgery was scheduled to be performed in (b)(6) 2020 (date of surgery was not fixed yet).The surgery was closed by 100 minutes surgical delay.The patient had to stay in bed due to lack of stem in femur, and so there was concerns about muscle and soft tissue contractures.Doctors comments: the revision surgery was able to complete only once if the stem and sleeve had separated and the new stem had been replaced.Please investigate why the stem and the sleeve did not separate.No further information is available.

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: the device was reviewed by bioengineering and report was received stating: it is unlikely that a potential product issue was present root cause undetermined.Depuy synthes considers the investigation closed at this time.Should additional information be received, the information will be reviewed and the investigation may be re-opened as necessary.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. .

• Type of Device: S-ROM HIP SYSTEM : HIP FEMORAL SLEEVE
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 9581281
• MDR Text Key: 185849820
• Report Number: 1818910-2020-01574
• Device Sequence Number: 1
• Product Code: LPH
• UDI-Device Identifier: 10603295175179
• UDI-Public: 10603295175179
• Combination Product (y/n): N
• PMA/PMN Number: K934412
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,health professional,o
• Type of Report: Initial,Followup,Followup
• Report Date: 12/25/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/13/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 55-0501
• Device Catalogue Number: 550501
• Device Lot Number: 3176504
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/24/2020
• Date Manufacturer Received: 02/20/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention