| Date Initiated by Firm | January 26, 2016 |
| Create Date | April 14, 2016 |
| Recall Status1 |
Terminated 3 on October 27, 2016 |
| Recall Number | Z-1497-2016 |
| Recall Event ID |
73339 |
| 510(K)Number | K110804 K123716 |
| Product Classification |
Tubes, gastrointestinal (and accessories) - Product Code KNT
|
| Product | AMT G-Jet Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm SINGLE USE ONLY Rx ONLY STERILE.
For use in patients who cannot absorb adequate nutrition through the stomach. |
| Code Information |
Model #GJ-1415-45, Lot # 15104750, Exp Date: 2018/09 |
| FEI Number |
1526012
|
Recalling Firm/ Manufacturer |
Applied Medical Technology Inc 8000 Katherine Blvd Brecksville OH 44141-4202
|
| For Additional Information Contact | 440-717-4000 |
Manufacturer Reason for Recall | The firm received complaints that the product is shorter in length than indicated on the label. |
FDA Determined Cause 2 | Employee error |
| Action | On 1/26/2016 the firm telephoned their customers notifying them of the recall. On 2/19/2016 the firm sent recall notification letters to their customers. The letter identified the product, problem, and actions to be taken by the customer. |
| Quantity in Commerce | 20 units |
| Distribution | Distributed in the states of AZ, CA, DE, IN, MI, NM, PA & VA. |
| 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 = KNT
|