MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2019-01-09 for 1.5 MM SYSTEM HIGH TORQUE (HT), SD, X-DR, SCR, 5/PK 1.5 MM X 4 MM N/A 95-6104 manufactured by Biomet Microfixation.
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(b)(4). Customer has indicated that the product is in process of being returned to zimmer biomet for investigation. Once the investigation has been completed, a follow-up mdr will be submitted.
 Patient Sequence No: 1, Text Type: N, H10
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It was reported the screw was unable to be gripped. Attempts have been made and no further information has been provided. No adverse events have been reported as a result of the malfunction.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0001032347-2019-00017 | 
| MDR Report Key | 8231060 | 
| Report Source | DISTRIBUTOR,FOREIGN,HEALTH PR | 
| Date Received | 2019-01-09 | 
| Date of Report | 2019-04-24 | 
| Date of Event | 2018-11-21 | 
| Date Mfgr Received | 2019-03-26 | 
| Date Added to Maude | 2019-01-09 | 
| Event Key | 0 | 
| Report Source Code | Manufacturer report | 
| Manufacturer Link | Y | 
| Number of Patients in Event | 0 | 
| Adverse Event Flag | 3 | 
| Product Problem Flag | 3 | 
| Reprocessed and Reused Flag | 3 | 
| Health Professional | 3 | 
| Initial Report to FDA | 3 | 
| Report to FDA | 3 | 
| Event Location | 3 | 
| Manufacturer Contact | MRS. MICHELLE COLE | 
| Manufacturer Street | 1520 TRADEPORT DRIVE | 
| Manufacturer City | JACKSONVILLE FL 32218 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 32218 | 
| Manufacturer Phone | 9047414400 | 
| Manufacturer G1 | BIOMET MICROFIXATION | 
| Manufacturer Street | 1520 TRADEPORT DRIVE | 
| Manufacturer City | JACKSONVILLE FL 32218 | 
| Manufacturer Country | US | 
| Manufacturer Postal Code | 32218 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | 1.5 MM SYSTEM HIGH TORQUE (HT), SD, X-DR, SCR, 5/PK 1.5 MM X 4 MM | 
| Generic Name | FASTENER, SCREW, CRANIOPLASTY | 
| Product Code | HBW | 
| Date Received | 2019-01-09 | 
| Returned To Mfg | 2019-03-19 | 
| Model Number | N/A | 
| Catalog Number | 95-6104 | 
| Lot Number | UNKNOWN | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | R | 
| Device Age | DA | 
| Device Eval'ed by Mfgr | Y | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | BIOMET MICROFIXATION | 
| Manufacturer Address | 1520 TRADEPORT DRIVE JACKSONVILLE FL 32218 US 32218 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 2019-01-09 |