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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

LSL Healthcare Medical Procedure Kits Recalled for Non-Sterile Alcohol Pads

Agency Publication Date: April 22, 2026
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Summary

LSL Healthcare Inc. is recalling approximately 10,060 medical procedure kits because they contain Webcol Large Alcohol Prep Pads that were recalled for not being sterile. These kits, including Central Line Dressing, IV Start, and Urine Collection kits, were distributed across Maryland, Illinois, and Minnesota. Using non-sterile components in medical procedures can lead to serious infections, although no injuries have been reported to date.

Risk

The alcohol prep pads inside these kits may contain bacteria or other contaminants instead of being sterile, which can introduce pathogens directly into a patient's bloodstream or urinary tract during a procedure. This poses a significant risk of infection, especially for patients with weakened immune systems or those receiving central line care.

What You Should Do

  1. Identify if you have any of the affected LSL Healthcare kits by checking the Model Numbers (2717H, 2717J, 1555, 2925H, 3131, or 7554) and the associated lot numbers and expiration dates. See the Affected Products section below for the full list of affected codes.
  2. Stop using the recalled medical kits immediately.
  3. Contact the manufacturer, LSL Healthcare Inc., or your medical supply distributor to arrange for the return, replacement, or correction of the kits.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 if you have additional questions regarding this device recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: LSL Healthcare Central Line Dressing Kit
Model / REF:
2717H
Lot Numbers:
6A3181 (Exp 11/30/2026)
UDI:
00661392054738
GTIN:
00661392054738

Contains recalled Webcol Large Alcohol Prep Pads.

Product: LSL Healthcare Standard Central Line Dressing Change Kit
Model / REF:
2717J
Lot Numbers:
6A3043 (Exp 11/30/2026)
6B3076 (Exp 01/31/2027)
UDI:
00661392054721
GTIN:
00661392054721

Contains recalled Webcol Large Alcohol Prep Pads.

Product: LSL Healthcare Foley Urine Collection Kit
Model / REF:
1555
Lot Numbers:
260221 (Exp 02/28/2027)
UDI:
00661392002326
GTIN:
00661392002326

Contains recalled Webcol Large Alcohol Prep Pads.

Product: LSL Healthcare Infant Central Line Dressing Change Kit
Model / REF:
2925H
Lot Numbers:
6B3022 (Exp 11/30/2026)
UDI:
00661392052635
GTIN:
00661392052635

Contains recalled Webcol Large Alcohol Prep Pads.

Product: LSL Healthcare IV Start Kit
Model / REF:
3131
Lot Numbers:
6A3139 (Exp 01/21/2028)
UDI:
00661392054271
GTIN:
00661392054271

Contains recalled Webcol Large Alcohol Prep Pads.

Product: LSL Healthcare Wound Closure Tray
Model / REF:
7554
Lot Numbers:
6A3146 (Exp 01/22/2028)
UDI:
00661392008342
GTIN:
00661392008342

Contains recalled Webcol Large Alcohol Prep Pads.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98631
Status: Active
Manufacturer: LSL Healthcare Inc.
Sold By: LSL Healthcare Inc.
Manufactured In: United States
Units Affected: 10,060
Distributed To: Maryland, Illinois, Minnesota

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.