ANCHORAGE PLSS3020Recalls & reported problems
Stryker GmbH · Non Locking Screw · Class 2 · Implant
All models of ANCHORAGE (52)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613252262725), received between Jun 6, 2019 and Jun 6, 2019 — classified as 4 injuries.
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem4
Patient problems
- Tissue Damage3
- No Code Available1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryJun 6, 2019Adverse Event Without Identified Device or Use Problem
SURGEON REPORTED THAT HE REMOVED A ANCHORAGE PLATE ON FRIDAY (B)(6) 2019. ON REMOVAL HE NOTICED WHAT APPEARED TO DARKENED TISSUE AROUND THE PLATE AND SCREW INTERFACE.
Patient problems: No Code Available
MAUDE report 8675265 ↗InjuryJun 6, 2019Adverse Event Without Identified Device or Use Problem
SURGEON REPORTED THAT HE REMOVED A ANCHORAGE PLATE ON FRIDAY (B)(6) 2019. ON REMOVAL HE NOTICED WHAT APPEARED TO DARKENED TISSUE AROUND THE PLATE AND SCREW INTERFACE.
Patient problems: Tissue Damage
MAUDE report 8675191 ↗InjuryJun 6, 2019Adverse Event Without Identified Device or Use Problem
SURGEON REPORTED THAT HE REMOVED A ANCHORAGE PLATE ON FRIDAY(B)(6) 2019. ON REMOVAL HE NOTICED WHAT APPEARED TO DARKENED TISSUE AROUND THE PLATE AND SCREW INTERFACE.
Patient problems: Tissue Damage
MAUDE report 8675187 ↗InjuryJun 6, 2019Adverse Event Without Identified Device or Use Problem
SURGEON REPORTED THAT HE REMOVED A ANCHORAGE PLATE ON FRIDAY (B)(6) 2019. ON REMOVAL HE NOTICED WHAT APPEARED TO DARKENED TISSUE AROUND THE PLATE AND SCREW INTERFACE.
Patient problems: Tissue Damage
MAUDE report 8675087 ↗
Other PLATE, FIXATION, BONE devices
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- PRECICE® Plating System LP4.5-PRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls6 reports
- PRECICE® Plating System LP4.5-MLT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls5 reports
- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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