TMS SYSTEM 25-2007Recalls & reported problems
Biomet Microfixation, Inc · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00841036089405), received between Jul 9, 2020 and Nov 24, 2020 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (1 report).
11 other recalls cover devices cleared under the same FDA submission (K121589, K121624, K953385); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Device-Device Incompatibility1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
- Unspecified Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 24, 2020Device-Device Incompatibility; Device-Device Incompatibility
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient
MAUDE report 10896403 ↗MalfunctionOct 5, 2020Material Deformation; Material Deformation
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10626188 ↗InjuryJul 9, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION.
Patient problems: Unspecified Infection
MAUDE report 10253232 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K121589, K121624, K953385. One submission often covers many models, so check the product and lot details in each record.
- Z-1220-2017 · Jan 10, 2017 · Terminated1.5mm System, Cranio-maxillofacial Bone Screws 1.5 x 4mm HT SD X-DR Screw, Bone Screw
- Z-0137-2016 · Aug 6, 2015 · TerminatedThinflap System Case The cases hold surgical instrumentation in place during handling and storage.
- Z-0136-2016 · Aug 6, 2015 · TerminatedNeuro Combo Set Case The cases hold surgical instrumentation in place during handling and storage.
- Z-0835-2012 · Nov 8, 2010 · TerminatedPackage of cross-drive bone screws labeled in part: "***REF #95-1504***"1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, 5/ PK***1.5 X4MM TITANIUM***CAUTION: FEDERAL LAW RESTRICTS
- Z-0836-2012 · Nov 8, 2010 · TerminatedPackage of center-drive bone screws labeled in part: "***REF: 01-7204***1.5MM" SYSTEM CENTER-DRIVE SCREW, 5/ PKG***1.5 X4MM TITANIUM***CAUTION: FEDERAL LAW RESTRICTS THIS DEVICE T
- Z-2385-2011 · Jul 28, 2010 · Terminated***BIOMET MICROFIXATION BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSONVILLE, FL 32218 USA www.biometmicrofixation.com***6 HOLE REGULAR DOUBLE Y PLATE***"1.5MM SYSTEM PLATE DOUBL
- Z-2873-2011 · May 17, 2010 · Terminated"***REF: 91-6704***THINFLAP SYSTEM CROSS-DRIVE, SELF-DRILLING SCREW 1.5X4MM (.059X.159") (WXL)***TITANIUM***NON-STERILE PRODUCT***BIOMET MICROFIXATION 1520 TRADEPORT DRIVE JACKSON
- Z-1286-2012 · Apr 26, 2010 · TerminatedProduct is labeled in part: "***REF: 01-7036, LOT 999999, "1.5MM" SYSTEM PLATE L-SHAPE, 3 X 3 HOLE, 100 DEGREE, QTY 00001, CE 0086, 2010-04 *** NON-STERILE PRODUCT ***, LEFT, X-L
- Z-2206-2010 · Mar 17, 2010 · TerminatedBIOMET MICROFIXATION "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW, QTY 1, 1.5 X 4MM TITANIUM. REF 91-1504 1 COUNT and REF 95-1504 - 5 PACK. BIOMET MICROFIXATION 1520 TRADEPO
- Z-1151-2010 · Oct 6, 2009 · TerminatedBIOMET MICROFIXATION, "1.5MM" SYSTEM BONE SCREW LP, SELF DRILL, X-DRIVE, SGL.LEAD AUGER POINT, 1.5 X 3.5MM, TITANIUM, NON STERILE PRODUCT. Model 01-7293 and 99-7293-01. BIOMET MI
- Z-1943-2010 · Oct 5, 2009 · TerminatedBIOMET MICROFIXATION REF: 91-6103 "1.5MM" SYSTEM HIGH TORQUE (HT), SD, X-DR, SCREW 1.5MM X 3.5MM (WXL) TITANIUM LOT 829760, ***NON STERILE PRODUCT***. Bone screws used along with
Other COVER, BURR HOLE devices
- GUARDIAN™ 6010St. Jude Medical, Inc. · COVER, BURR HOLE151 reports
- GUARDIAN™ 6010St. Jude Medical, Inc. · COVER, BURR HOLE1 death25 reports
- "1.5MM" SYSTEM 95-1505Biomet Microfixation, Inc · COVER, BURR HOLE23 reports
- "1.5MM" SYSTEM 91-6105Biomet Microfixation, Inc · COVER, BURR HOLE20 reports
- CRANIOFIX® ABSORBABLE FF016Aesculap AG · COVER, BURR HOLE8 reports
- "1.5MM" SYSTEM 91-6106Biomet Microfixation, Inc · COVER, BURR HOLE7 reports
- 1.5MM SYSTEM 91-6105X-50Biomet Microfixation, Inc · COVER, BURR HOLE6 reports
- 1.5MM SYSTEM 01-7114Biomet Microfixation, Inc · COVER, BURR HOLE2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.