Certain Cover Screw Dental implants
Biomet 3i
Pouches may not have been sealed during packing.
Medical equipment, implants, and diagnostic devices
Biomet 3i
Pouches may not have been sealed during packing.
DePuy Synthes is voluntarily initiating a recall due to a possibility the fastener on the Titanium Single Vector Distractor Body may become prematurely separated from the Proximal Foot Plate.
Hospira has become aware of customers using the incorrect size Receptal liners with their Receptal canisters, e.g., 1.5 L liner, 2L liner or 3L liner with a 1L canister. It is possible that if an incorrectly sized liner is used with a different size canister the lid may not fit and the vacuum/suction will not be sufficient and/or consistent.
Pouches may not have been sealed during packing.
Biomet 3i
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Biomet 3i
Pouches may not have been sealed during packing.
Biomet 3i
Pouches may not have been sealed during packing.
Biomet 3i
Pouches may not have been sealed during packing.
Stanmore Implants Worldwide
The manufacturer has identified that the stated Femoral Plateau Plates may not fit into the intended Femoral Knee mating component and thus sit flush upon the Femoral Knee component prior to implantation.
Potential for compromise of the package resulting in a breach of the sterile barrier
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Straumann Manufacturing
Misalignment with the Loxim transfer piece markings, the positioning of the implant will be incorrect for optimal restoration
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Biomet 3i
Pouches may not have been sealed during packing.
Biomet 3i
Pouches may not have been sealed during packing.