
Smith and Nephew · Model Dyonics POWER Small Joint Shaver
Dyonics POWER Small Joint Shaver Handpiece.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Handpiece runs slow, stalls when drilling / cutting, or does not run at all.
Root cause: Worn motor / turbine, worn gears / bearings, a low or aged battery, or (pneumatic) low supply pressure / a worn hose.
Symptoms: Handpiece or attachment gets hot quickly, burn / thermal-necrosis risk.
Root cause: Worn bearings / gears, a dry / seized attachment, or over-duty use.
Symptoms: Few cases per charge, will not reach full charge, sudden shutdown.
Root cause: Aged battery pack or a charger fault.
Symptoms: Bur / blade / pin slips or will not lock, attachment wobbles, quick-coupler worn.
Root cause: Worn chuck / collet or coupling.
Symptoms: Speed will not vary, forward/reverse or oscillate will not select, trigger sticks.
Root cause: Worn trigger / control mechanism or its seals.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Motor / turbine assembly | Periodic replacement | $$$ | Difficult |
| Gear / bearing service kit | Periodic replacement | $$ | Difficult |
| Battery pack (battery tools) | Periodic replacement | $$$ | Fairly easy |
| Chuck / collet / quick-coupler | Periodic replacement | $$ | Moderate |
| Trigger / seal kit | Periodic replacement | $$ | Moderate |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
No documents available for this device yet.
Synced live from the FDA openFDA API.
Multiple or incorrect expiration dates were provided on the affected designation labels.
The 4.5MM PeriLoc Targeter right hand part was anodized green and was marked as a left-hand part.
The spike rail was manufactured with an oversized thru-hole which could potentially cause the dowel pin to fall out and the device to disassemble.
In rare circumstances, when surgeons use the software to plan the strut adjustment, an inverted image of the frame is generated by the software. The frame will appear inverted in the preview images on the Strut Settings tab.
Devices, incorrectly labeled as a VLP MINI-MOD 2.0MM STRAIGHT PLATE 8 HOLE, contained a VLP MINI-MOD 2.0MM STOUT PLATE 8 HOLE and vice versa
One lot of EVOS 2.4MM Flex Plate 6 Hole packaging contained templates.
All lots of modular neck hip prostheses are being recalled due to a higher than anticipated complaint and adverse event trend.
The labels correctly state that the product should be a 25mm screw, but the box contained a longer, 35mm screw.
The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had revision rates which were higher than established benchmarks.
The R3 Constrained outer liner locking groove diameter is 0.030 inches oversized and may not allow the locking ring to engage into the R3 shell.
Devices labeled with an expiry period of 48 months instead of 36 months; an additional 12 months for which product and package reliability has not been validated.
Product has insufficient weld between the shaft tube and tip, could result in the tip separating from the shaft tube during use.
Smith & Nephew, Inc., St. Petersburg, FL is recalling multiple lot numbers of the following products: REMOVE Universal Adhesive Remover Wipes, UNI-SOLVE Adhesive Remover Wipes, SKIN-PREP Protective Wipes, PERI-PREP Protective Wipes, and NO-STING SKIN-PREP Protective Wipes. These products were manufactured by H&P Industries dba The Triad Group who has initiated a recall of products manufactured i
During the manufacturing process for several batches of R3 Ceramic Liners, the titanium rings were pressed onto the ceramic component with a higher force than allowed by manufacturing specifications. This has the potential to result in lower than expected strength for the liners.
Inner packaging of sterile product was not sealed. Lack of sterility assurance.
Product sterility is compromised due to breach in the sterile packaging.
Hinge failure: The product is cracking or breaking during use.
Incorrect labeling. Kit labels may incorrectly state that a flat drain is contained as a kit component while some kits may contain a round drain.
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