MultiQuant MD software where under certain conditions a user can be presented with incorrect quantitative results when using the Sum Multiple Ions feature.
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Medical Devices Recalls
Medical equipment, implants, and diagnostic devices
38,779 Total Recalls
Class I - Dangerous
Pouches may not have been sealed during packing.
Potential for compromise of the package resulting in a breach of the sterile barrier
Class I - Dangerous
Pouches may not have been sealed during packing.
Class I - Dangerous
Pouches may not have been sealed during packing.
Class I - Dangerous
Pouches may not have been sealed during packing.
Class I - Dangerous
Pouches may not have been sealed during packing.
Class I - Dangerous
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.
MAMMOGRAPHY
Avid Medical
Class I - Dangerous
Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.
Class I - Dangerous
Pouches may not have been sealed during packing.
Prep-Tite Post Dental implants
Biomet 3i
Class I - Dangerous
Pouches may not have been sealed during packing.
Titanium Hexed Uniscrew Dental implants
Biomet 3i
Class I - Dangerous
Pouches may not have been sealed during packing.
Class I - Dangerous
Pouches may not have been sealed during packing.
Potential for compromise of the package resulting in a breach of the sterile barrier
Class I - Dangerous
Pouches may not have been sealed during packing.
EP Healing Abutment Dental implants
Biomet 3i
Class I - Dangerous
Pouches may not have been sealed during packing.
Class I - Dangerous
TRYX products are being recalled since the processes of spaying, welding, drying oven and polymer were not adequately validated.
Class I - Dangerous
Pouches may not have been sealed during packing.
Class I - Dangerous
Profemur(R) neck, Item Number PHA01222 (Short AR VV2 Ti Neck) was labeled as Item Number PHA01212 (Short AR VV1 Ti Neck).
Potential for compromise of the package resulting in a breach of the sterile barrier