ANCHORAGERecalls & reported problems across all models
Stryker GmbH · 52 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 180
- Deaths reported
- 0
- Injuries reported
- 122
- Recalls
- 0
We found 52 models of ANCHORAGE by Stryker GmbH in the FDA's device registry (GUDID). Together they are named in 180 adverse event reports in the FDA's MAUDE database, received between May 2, 2017 and Sep 10, 2026 — classified as 122 injuries, 58 malfunctions.
The most frequently reported specific device problem is “Fracture” (26 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported ANCHORAGE problems
Device problems
- Adverse Event Without Identified Device or Use Problem86
- Fracture26
- Break17
- Dull, Blunt16
- Positioning Failure10
- Migration9
- Difficult to Insert6
- Structural Problem4
Patient problems
- Pain73
- No Clinical Signs, Symptoms or Conditions25
- Insufficient Information17
- No Known Impact Or Consequence To Patient17
- Failure of Implant14
- Nonunion/Delayed-union Bone Fracture9
- No Consequences Or Impact To Patient8
- Post Operative Wound Infection7
ANCHORAGE models
52 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ANCHORAGE 626892Plate, fixation, bone16 reports
- ANCHORAGE 705172Plate, fixation, bone16 reports
- ANCHORAGE PLP14341PLATE, FIXATION, BONE8 reports
- ANCHORAGE PLP14342PLATE, FIXATION, BONE8 reports
- ANCHORAGE PLSL3514PLATE, FIXATION, BONE7 reports
- ANCHORAGE PLP10341PLATE, FIXATION, BONE6 reports
- ANCHORAGE PLP11342PLATE, FIXATION, BONE6 reports
- ANCHORAGE PLP30171PLATE, FIXATION, BONE6 reports
- ANCHORAGE PLP40280PLATE, FIXATION, BONE6 reports
- ANCHORAGE PLSL3014PLATE, FIXATION, BONE6 reports
- ANCHORAGE PLP30172PLATE, FIXATION, BONE5 reports
- ANCHORAGE PLP30202PLATE, FIXATION, BONE5 reports
- ANCHORAGE PLP30201PLATE, FIXATION, BONE5 reports
- ANCHORAGE PLP10461PLATE, FIXATION, BONE4 reports
- ANCHORAGE PLP11341PLATE, FIXATION, BONE4 reports
- ANCHORAGE PLP20341PLATE, FIXATION, BONE4 reports
- ANCHORAGE PLSS3020PLATE, FIXATION, BONE4 reports
- ANCHORAGE PLSS3522PLATE, FIXATION, BONE4 reports
- ANCHORAGE 626891Plate, fixation, bone4 reports
- ANCHORAGE 626895Plate, fixation, bone4 reports
- ANCHORAGE PLP10342PLATE, FIXATION, BONE3 reports
- ANCHORAGE PLP20342PLATE, FIXATION, BONE3 reports
- ANCHORAGE PLP40340PLATE, FIXATION, BONE3 reports
- ANCHORAGE PLP40400PLATE, FIXATION, BONE3 reports
- ANCHORAGE PLSS3030PLATE, FIXATION, BONE3 reports
- ANCHORAGE 626894Plate, fixation, bone3 reports
- ANCHORAGE PLP10462PLATE, FIXATION, BONE2 reports
- ANCHORAGE PLP21341PLATE, FIXATION, BONE2 reports
- ANCHORAGE PLP50230PLATE, FIXATION, BONE2 reports
- ANCHORAGE PLSL3010PLATE, FIXATION, BONE2 reports
- ANCHORAGE PLSL3012PLATE, FIXATION, BONE2 reports
- ANCHORAGE PLSL3028PLATE, FIXATION, BONE2 reports
- ANCHORAGE PLSL3516PLATE, FIXATION, BONE2 reports
- ANCHORAGE PLSS3520PLATE, FIXATION, BONE2 reports
- ANCHORAGE PLP30141PLATE, FIXATION, BONE1 report
- ANCHORAGE PLP30142PLATE, FIXATION, BONE1 report
- ANCHORAGE PLP40160PLATE, FIXATION, BONE1 report
- ANCHORAGE PLP40220PLATE, FIXATION, BONE1 report
- ANCHORAGE PLSL3016PLATE, FIXATION, BONE1 report
- ANCHORAGE PLSL3018PLATE, FIXATION, BONE1 report
- ANCHORAGE PLSL3020PLATE, FIXATION, BONE1 report
- ANCHORAGE PLSL3520PLATE, FIXATION, BONE1 report
- ANCHORAGE PLSL3524PLATE, FIXATION, BONE1 report
- ANCHORAGE PLSL3522PLATE, FIXATION, BONE1 report
- ANCHORAGE PLSS3016PLATE, FIXATION, BONE1 report
- ANCHORAGE PLSS3022PLATE, FIXATION, BONE1 report
- ANCHORAGE PLSS3024PLATE, FIXATION, BONE1 report
- ANCHORAGE XFR006100INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- ANCHORAGE XTV008001ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ANCHORAGE XVIMQ001020ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ANCHORAGE 626893Plate, fixation, bone1 report
- ANCHORAGE 626898Plate, fixation, bone1 report
Recent ANCHORAGE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 10, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50716214 ↗MalfunctionSep 7, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50652062 ↗InjuryJun 25, 2026Fracture
IT WAS REPORTED THAT A FEW MONTHS AFTER THE SURGERY, THE PLATE BROKE. THE PATIENT UNDERWENT A REVISION SURGERY.
Patient problems: Insufficient Information
MAUDE report 25626834 ↗MalfunctionApr 20, 2026Dull, Blunt
AS REPORTED: "USED BOTH REAMERS AND THEY WERE NOT REAMING. VERY DULL."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24922339 ↗MalfunctionApr 20, 2026Dull, Blunt
AS REPORTED: "USED BOTH REAMERS AND THEY WERE NOT REAMING. VERY DULL."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24922337 ↗InjuryMar 5, 2026Migration
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT 142 HAD DEVICE DISPLACEMENT AND GENERALIZED PAIN
Patient problems: Pain
MAUDE report 24518440 ↗InjuryMar 5, 2026Migration
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN (B)(6) 2016 ¿ (B)(6) 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT 142 HAD DEVICE DISPLACEMENT AND GENERALIZED PAIN
Patient problems: Pain
MAUDE report 24518437 ↗InjuryMar 5, 2026Migration
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN (B)(6) 2016 ¿ (B)(6) 2025DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT 102 HAD DEVICE DISPLACEMENT.
Patient problems: Insufficient Information
MAUDE report 24518053 ↗InjuryMar 5, 2026Adverse Event Without Identified Device or Use Problem
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT 19 HAD GENERALIZED PAIN.
Patient problems: Pain
MAUDE report 24517761 ↗InjuryMar 5, 2026Adverse Event Without Identified Device or Use Problem
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT 77 HAD GENERALIZED PAIN.
Patient problems: Pain
MAUDE report 24517757 ↗InjuryMar 5, 2026Migration
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT 7 HAD DEVICE DISPLACEMENT.
Patient problems: Insufficient Information
MAUDE report 24517185 ↗InjuryMar 5, 2026Fracture
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT (B)(6) HAD DEVICE BREAKAGE.
Patient problems: Insufficient Information
MAUDE report 24517027 ↗InjuryMar 5, 2026Fracture
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT (B)(6) HAD DEVICE BREAKAGE.
Patient problems: Insufficient Information
MAUDE report 24517023 ↗InjuryMar 4, 2026Adverse Event Without Identified Device or Use Problem
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT (B)(6) HAD GENERALIZED PAIN.
Patient problems: Pain
MAUDE report 24504279 ↗InjuryMar 4, 2026Adverse Event Without Identified Device or Use Problem
THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT (B)(6) HAD GENERALIZED PAIN.
Patient problems: Pain
MAUDE report 24504278 ↗
Other Stryker GmbH products
All Stryker GmbH devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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