Prismatik Dentalcraft, Inc. has recalled 15 units of the Glidewell HT Implant Twist Drill (Ø1.5 x 8 mm) because of a packaging error where the wrong device was placed inside the labeled container. These surgical drills are used by dental professionals to prepare bone sites for dental implants. Although no injuries have been reported, the recall was initiated to prevent surgical complications resulting from using an incorrect drill size.
A packaging mix-up can lead a dental professional to use a drill that does not match the intended surgical plan. This could result in an improperly sized or positioned implant site, leading to surgical delays or injury to the patient's jaw or surrounding tissue.
The initial Twist Drill is used to deepen the osteotomy and establish the trajectory of subsequent drills in the placement of a dental implant.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
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Sources: FDA iRES · Raw API Response
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