LSL Healthcare Wound Closure Tray Model 7554 Recalled for Non-Sterility
LSL Healthcare is recalling its Wound Closure Tray (Model 7554) distributed nationwide to Maryland, Illinois, and Minnesota because the kits contained non-sterile Webcol Large Alcohol Prep Pads.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II recall involving non-sterility of medical devices used in wound closure procedures presents a potential risk of infection or adverse health consequences. No illnesses or injuries are reported in the source text, but the hazard (non-sterile medical-grade equipment) is significant and warrants High severity per the rubric.
Plain-English summary
LSL Healthcare Inc. is recalling the Wound Closure Tray, Model/Catalog Number 7554, distributed in the United States, specifically in Maryland, Illinois, and Minnesota. The recall was initiated because medical procedure kits contained Webcol Large Alcohol Prep Pads that were subsequently recalled for non-sterility.
The affected product (Lot#6A3146, Expiration Date 01/22/2028) was distributed in a quantity of 200 units. The UDI-DI is 00661392008342.
Healthcare facilities and users who have received this product should stop using the affected Wound Closure Tray kits and contact LSL Healthcare Inc. for instructions on product return or replacement. Patients who may have been exposed to non-sterile preparation pads should consult with their healthcare provider.
The recalled product
- Product
- LSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554
- Manufacturer
- LSL Healthcare Inc.
- Affected units
- 200
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Lot Code: Model No. 7554
- UDI-DI 00661392008342
- Lot#6A3146
- Expiration Date 01/22/2028 GTIN: (01)00661392008342(10)6A3146(17)280122
Distribution
Part of a larger recall action
This product is one of 6 recalled by LSL Healthcare Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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