MAUDE Adverse Event Report: ZIMMER BIOMET, INC. COMPR 8MM HUM FRACT STEM PPS; EXTREMITIES, IMPLANT

Model Number	N/A
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Tissue Damage (2104); Tingling (2171); Numbness (2415)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Concomitant medical devices: item#115370; lot# 666100; comp rvs tray co 44mm; item# xl-115363; lot# 298700; arcom xl 44-36 std hmrl brng; item# 115310; lot# 892640; comp rvrs shldr glnsp std 36mm; item# 010000589; lot# 409640; comp rvrs 25mm bsplt ha+adptr; item# 115396; lot# 783340; comp rvs cntrl 6.5x30mm st/rst; item# 180552; lot# 527240; comp lk scr 3.5hex 4.75x25 st; item# 180552; lot# 900780; comp lk scr 3.5hex 4.75x25 st; item# 180550; lot# 563630; comp lk scr 3.5hex 4.75x15 st.Foreign: event occurred in (b)(6).The product will not be returned to zimmer biomet for investigation.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.Multiple mdr reports were filed for this event, please see associated reports: 0001825034-2020-03809, 0001825034-2020-03811, 0001825034-2020-03812, 0001825034-2020-03814, 0001825034-2020-03815, 0001825034-2020-03816, 0001825034-2020-03817, 0001825034-2020-03818.Remains implanted.
Event or Problem Description
It was reported that a patient underwent an initial left reverse shoulder procedure.Subsequently, the patient claims to be experiencing tingling, numbness, loss of range of motion, torn rotator cuff and nerve damage.Attempts have been made and additional information on the reported event is unavailable at this time.No additional patient consequences were reported.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.Reported event was unable to be confirmed due to limited information received from the customer.Device history record was reviewed and no discrepancies were found.Root cause was unable to be determined as the necessary information to adequately investigate the reported event was not provided.A summary of the investigation has been sent to the complainant.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmerbiomet will continue to monitor for trends.
Event or Problem Description
No further event information available at the time of this report.

• Brand Name: COMPR 8MM HUM FRACT STEM PPS
• Common Device Name: EXTREMITIES, IMPLANT
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 56 e. bell drive; warsaw IN 46582
• MDR Report Key: 10682951
• Report Number: 0001825034-2020-03813
• Device Sequence Number: 436596
• Product Code: KWS
• UDI-Device Identifier: 00880304591547
• UDI-Public: (01)00880304591547
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K140652
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 02/10/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: 12-113558
• Device Lot Number: 224320
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 09/22/2020
• Supplement Date Received by Manufacturer: 02/04/2021
• Initial Report FDA Received Date: 10/15/2020
• Supplement Report FDA Received Date: 02/11/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: N/A
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Weight: 48