Data Foundry

Medical device recalls 2020

Snappy Abutment 5 — Class II medical device recall Z-1855-2020

Terminated recall by Nobel Biocare Usa Llc, reported 2020-05-13, distributed nationwide. Packages of abutments may contain an incorrect screw. While the screw will tighten, it cannot be guaranteed th

Recall numberZ-1855-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmNobel Biocare Usa Llc, Yorba Linda, CA, United States
Recall initiated2019-08-09
Classified2020-05-04
Reported by FDA2020-05-13
Terminated2021-12-01
DistributedNationwide (US)
Quantity215 units
UPC / GTIN / UDI-DI07332747034264
Lot numbers13077700
Model numbers36683

Product

Snappy Abutment 5.5 CC RP 3 mm; pre-manufactured prosthetic components directly connected to the endosseous implant, catalog no. 36683 - - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to restore chewing function.

Reason for recall

Packages of abutments may contain an incorrect screw. While the screw will tighten, it cannot be guaranteed that the screw will not loosen. In case the screw loosens the abutment should be retightened with the correct screw.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1855-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.