FDAClass IIJanuary 26, 2022

Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 recall: Labeling Error

Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107

Why was Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 recalled?

Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 has an implant with measure of 3.5x13mm; and Carton Box (138.107- Easypack Helix GM Acqua has a 3.5x8mm implant instead of a 3.5x 13mm implant

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot GNV20: UDI:7899878052906

Product
Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107
Recalling firm
Straumann USA LLC
Quantity
1 unit
Distribution
US Nationwide Distribution in the states of FL, IL, OH
Recall date
January 26, 2022
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls