MAUDE Adverse Event Report: ZIMMER BIOMET, INC. JGRKNT 2.9MM #2 BLUE MB SNGL NGLE; FASTENER, FIXATION

Model Number N/A

Device Problem Device Dislodged or Dislocated (2923)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 08/19/2021

Event Type  malfunction  

Manufacturer Narrative

(b)(4).Report source- (b)(6).Customer has indicated that the product will not be returned to zimmer biomet for investigation, as the device has been discarded.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.

Event Description

It was reported that the anchor pulled out when the surgeon pulled it lightly after insertion during surgery.The surgeon used another device.The device was discarded at the hospital.Attempts have been made and there is no further information at this time.

Manufacturer Narrative

Upon receipt of additional information it has been determined that this event has not caused or contributed to serious injury.The initial report was forwarded in error and can be voided.

Event Description

Upon receipt of additional information it has been determined that this event has not caused or contributed to serious injury.The initial report was forwarded in error and can be voided.

• Brand Name: JGRKNT 2.9MM #2 BLUE MB SNGL NGLE
• Type of Device: FASTENER, FIXATION
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 56 e. bell drive; warsaw IN 46582
• MDR Report Key: 12488079
• MDR Text Key: 271904554
• Report Number: 0001825034-2021-02672
• Device Sequence Number: 1
• Product Code: JDR
• Combination Product (y/n): N
• PMA/PMN Number: NI
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,health professional
• Type of Report: Initial,Followup
• Report Date: 10/14/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/17/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: 912029
• Device Lot Number: P14284
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 10/13/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Removal/Correction Number: N/A
• Patient Sequence Number: 1