MP Reconstruction ProsthesisRecalls & reported problems across all models
WALDEMAR LINK GmbH & Co. KG · 8 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one MP Reconstruction Prosthesis model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 8
- Recalls
- 1
We found 8 models of MP Reconstruction Prosthesis by WALDEMAR LINK GmbH & Co. KG in the FDA's device registry (GUDID). Together they are named in 9 adverse event reports in the FDA's MAUDE database, received between Mar 23, 2022 and Jun 12, 2026 — classified as 8 injuries, 1 malfunction.
The most frequently reported specific device problem is “Fracture” (5 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
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
MP Reconstruction Prosthesis recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Dec 5, 2024Open, Classified
Error on the main label and the patient label. The labels indicate a size XXL, this is a standard-size neck segment.. All further information on the labels is correct (Length, CCD and Offset).
Z-0769-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported MP Reconstruction Prosthesis problems
Device problems
- Fracture5
- Detachment of Device or Device Component2
- Inaccurate Information1
- Insufficient Device Problem Information1
- Off-Label Use1
Patient problems
- Failure of Implant4
- Insufficient Information2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Medical device site infection1
- No Clinical Signs, Symptoms or Conditions1
- Pain1
MP Reconstruction Prosthesis models
8 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MP Reconstruction Prosthesis 99-0984/32Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 recall1 report
- MP Reconstruction Prosthesis 172-921/14Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented2 reports
- MP Reconstruction Prosthesis 172-945/58Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- MP Reconstruction Prosthesis 172-921/20Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- MP Reconstruction Prosthesis 172-921/22Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- MP Reconstruction Prosthesis 172-918/16Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- MP Reconstruction Prosthesis 172-921/12Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
- MP Reconstruction Prosthesis 172-947/38Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented1 report
Recent MP Reconstruction Prosthesis adverse event reports
The 9 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJun 12, 2026Fracture
InjuryMay 27, 2026Fracture
InjuryMar 30, 2026Fracture
NOTIFIED BY A REPRESENTATIVE WHO WAS IN A PROCEDURE FOR AN EXTRACTION OF A DISTAL STEM FRACTURE. THE STEM WAS IMPLANTED IN 2014. THE REVISION WAS NOT A LINKBIO PRODUCT.
Patient problems: Failure of Implant
MAUDE report 24728219 ↗InjuryMar 17, 2026Fracture
NOTIFIED BY A REPRESENTATIVE WHO WAS IN A PROCEDURE FOR AN EXTRACTION OF A DISTAL STEM FRACTURE. THE STEM WAS IMPLANTED IN 2014. THE REVISION WAS NOT A LB PRODUCT.UNKNOWN EVENT DATE. THE EXTRACTED PRODUCT WAS DISCARDED. "[CUSTOMER]"
Patient problems: Insufficient Information
MAUDE report 24615507 ↗MalfunctionNov 26, 2024Inaccurate Information; Inaccurate Information
THE LABELS (MAIN LABEL AS WELL AS PATIENT LABEL) INDICATE A SIZE XXL, ALTHOUGH THIS IS A STANDARD-SIZE NECK SEGMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20785194 ↗InjuryMar 13, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
LOOSE EXPANSION SCREW AND NECK SEGMENT. [CUSTOMER, TRANSLATED FROM GERMAN].
Patient problems: Failure of Implant
MAUDE report 18892430 ↗InjuryAug 23, 2023Fracture; Fracture
InjuryApr 19, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
AN MP MODULAR STEM SYSTEM, ORIGINALLY IMPLANTED ON (B)(6) 2021, WAS REVISED BECAUSE OF INFECTION. THE IMPLANTS WERE REMOVED AND REPLACED WITH AN ANTIBIOTIC SPACER.
Patient problems: Medical device site infection
MAUDE report 16770520 ↗InjuryMar 23, 2022Off-Label Use; Detachment of Device or Device Component; Off-Label Use; Detachment of Device or Device Component
HIP REVISION: INSTABILITY OF THE PROSTHESIS.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Failure of Implant
MAUDE report 13858835 ↗
Other WALDEMAR LINK GmbH & Co. KG products
- Unicondylar Sled Prosthesis48 models · 12 reports · 48 recalls
- Endo-Model Modular Knee Prosthesis System64 models · 57 reports · 12 recalls
- LinkSymphoKnee117 models · 79 reports · 11 recalls
- LINK Instrument14 models · 8 reports · 12 recalls
- Endo-Model SL Knee Prosthesis System25 models · 52 reports · 6 recalls
- Endo-Model Standard Knee Prosthesis System15 models · 19 reports · 6 recalls
- LINK Embrace Shoulder System Line Extension2 models · 1 reports · 4 recalls
- SPII Model Lubinus174 models · 6 reports · 3 recalls
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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