MSS - Monobloc stemRecalls & reported problems across all models
Medacta International SA · 10 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one MSS - Monobloc stem model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 10 models of MSS - Monobloc stem by Medacta International SA in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
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
MSS - Monobloc stem 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.
- Apr 30, 2026Class IIOpen, Classified
Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are positioned approximately 0.2 mm per size more laterally than intended, which may increase the risk of fracture in the medial region of the proximal humerus.
Z-2618-2026 · Root cause: Device Design · names 10 of these models · Recall details · FDA record ↗
MSS - Monobloc stem models
10 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MSS - Monobloc stem 04.01.10.0970Orthopedic manual surgical instrument1 recall0 reports
- MSS - Monobloc stem 04.01.10.0971Orthopedic manual surgical instrument1 recall0 reports
- MSS - Monobloc stem 04.01.10.0972Orthopedic manual surgical instrument1 recall0 reports
- MSS - Monobloc stem 04.01.10.0973Orthopedic manual surgical instrument1 recall0 reports
- MSS - Monobloc stem 04.01.10.0974Orthopedic manual surgical instrument1 recall0 reports
- MSS - Monobloc stem 04.01.10.0975Orthopedic manual surgical instrument1 recall0 reports
- MSS - Monobloc stem 04.01.10.0976Orthopedic manual surgical instrument1 recall0 reports
- MSS - Monobloc stem 04.01.10.0977Orthopedic manual surgical instrument1 recall0 reports
- MSS - Monobloc stem 04.01.10.0978Orthopedic manual surgical instrument1 recall0 reports
- MSS - Monobloc stem 04.01.10.0979Orthopedic manual surgical instrument1 recall0 reports
Other Medacta International SA products
- GMK Sphere Total Knee System209 models · 2,306 reports
- GMK Primary Total Knee System99 models · 876 reports
- Shoulder System63 models · 716 reports
- AMIStem H Femoral Stems20 models · 679 reports
- Mpact Acetabular System68 models · 609 reports
- Mectacer Biolox Delta Femoral Ball Head15 models · 551 reports
- Quadra H femoral stems32 models · 354 reports
- MectaLIF Anterior6 models · 4 reports · 6 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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