| Date Initiated by Firm | September 28, 2017 |
| Create Date | February 27, 2018 |
| Recall Status1 |
Terminated 3 on October 05, 2020 |
| Recall Number | Z-0741-2018 |
| Recall Event ID |
78479 |
| 510(K)Number | K052501 |
| Product Classification |
Agent, tooth bonding, resin - Product Code KLE
|
| Product | Cosmedent's Etching Gel, 3g, 37% Phosphoric Acid, Rx only. Packaged in 3g Luer Lock syringes.
Used for etching enamel and dentin. |
| Code Information |
SKU #663-103, Lot No. 164222A, Exp. Date 10/31/2019 |
| FEI Number |
1450653
|
Recalling Firm/ Manufacturer |
Cosmedent, Inc. 4646 N Ravenswood Ave Chicago IL 60640-4510
|
| For Additional Information Contact | Gary Chuven 312-644-9365 |
Manufacturer Reason for Recall | Product packaged in a syringe that is not a lure lock syringe and the tip cold come off when expressing the material. |
FDA Determined Cause 2 | Under Investigation by firm |
| Action | Customers were sent recall notification letters on approximately 09/28/2017. The letter identified the affected device and discussed the reason for the recall. Instructions included discontinuing use of the product, and returning it to Cosmedent. The firm will issue a credit or refund for the recalled device. |
| Quantity in Commerce | 84 units |
| Distribution | Worldwide Distribution -- USA, to the states of IL, LA, MI, PA, and WI; and, to the countries of Australia, Hungary, and Spain. |
| Total Product Life Cycle | TPLC Device Report |
|
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
|
| 510(K) Database | 510(K)s with Product Code = KLE
|