FDA recall record

Straumann USA GM Helix Implant, REF: 109.984 recall — FDA Z-3173-2026

There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.

Class IIclassification
Z-3173-2026official record ID
Sep 23, 2026report date

Recall record at a glance

Official recordZ-3173-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmStraumann USA LLC
Report dateSep 23, 2026
Recall initiation dateAug 12, 2026
Quantity216
LocationAndover, MA, United States

Official product description

GM Helix Implant, REF: 109.984;

Why the product was recalled

There is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside.

Distribution information

US Nationwide distribution in the states of AL, AZ, CA, CO, FL, GA, IL, KS, LA, MA, MI, MO, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TX, VA, WI;

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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