LSL Healthcare Wound Closure Tray Recall - Non-Sterility, Lot 6A3146

Class 2 Device Recall LSL Healthcare Wound Closure Tray

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| | Class 2 Device Recall LSL Healthcare Wound Closure Tray | |

6200 W Howard St
Niles IL 60714-3404 |
| For Additional Information Contact | Demetrius Bridges
773-878-1100 Ext. 1120 |
| Manufacturer Reason
for Recall | Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility. |
| FDA Determined
Cause | Under Investigation by firm |
| Action | LSL Healthcare issued an UREGNT: Kit Component Recall to its consignees on 3/9/2026 via email. The notice explained the issue and requested the following:
"1. Immediately stop using the affected kits in your facility.
2. Inspection all inventory locations within your facility and destroy all affected kits according to your facility's disposal process. If immediate destruction is not feasible, the products should be quarantined until proper disposal can occur. If disposal is not possible, please request a Return Merchandise Authorization (RMA) to return these kits as indicated..
3. This recall should be executed at the distributor, hospital, and user levels. Identify all customers within your distribution network who may have purchased the affected products listed in this notification.
4. Complete the attached Response Form and return to the LSL contact provided on the form if you have any of the affected product in stock."
For assistance with this process, please contact your LSL representative or LSL at LSL Healthcare, 6200 W. Howard Street, Nile, IL 60714, (888)225-5575, LSLorderinquiries@lslhealcare.com. |
| Quantity in Commerce | 200 units |
| Distribution | US Nationwide distribution in the states of MD, IL, MN. |
| 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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes. | |