| Date Initiated by Firm | August 19, 2022 |
| Date Posted | November 11, 2022 |
| Recall Status1 |
Terminated 3 on March 20, 2023 |
| Recall Number | Z-0202-2023 |
| Recall Event ID |
90926 |
| 510(K)Number | K010607 |
| Product Classification |
System, irrigation, urological - Product Code LJH
|
| Product | MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001 |
| Code Information |
UDI/DI: 00628725001050, Lot Numbers: 159603, exp 2026-12-01 and 166945, exp 2027-06-01 |
| FEI Number |
3932
|
Recalling Firm/ Manufacturer |
Canadian Hospital Specialties 2760 Brighton Rd Oakville Canada
|
Manufacturer Reason for Recall | Some of the labels of the kits for product code 10-4001 in the specified lots have an illegible barcode which prevents successful scanning of the package. |
FDA Determined Cause 2 | Nonconforming Material/Component |
| Action | The firm issued a MEDICAL DEVICE RECALL NOTICE to its consignees on 08/23/2022 by email. The notice explained the issue and requested the following:
"TO IMPLEMENT THIS RECALL, PLEASE PERFORM THE FOLLOWING ACTIONS:
1.Examine your stock and determine if you have any affected product and lot.
2.Complete the attached Product Recall Response Form and send torecalls@chsltd.com.
3.Please report any affected units of the product to CHS for further instructions."
For questions, contact: recalls @chsltd.com |
| Quantity in Commerce | 9100 units |
| Distribution | US |
| 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 = LJH
|