The Recall Desk
HighFDA (Devices)·Z-1928-2026·Announced 2026-04-29

Central Line Dressing Kit containing non-sterile alcohol prep pads recalled

LSL Healthcare's Central Line Dressing Kit (Model 2717H) is being recalled because it contains Webcol Large Alcohol Prep Pads that were found to be non-sterile. The kits were distributed nationwide in Maryland, Illinois, and Minnesota.

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: This is an FDA Class II recall involving a sterile medical device (central line dressing kit) containing a recalled component with non-sterility. Non-sterile materials used in central line procedures pose a significant infection risk, meeting the "risk-of-harm" criterion; no reported illnesses or injuries are mentioned in the source text.

Plain-English summary

LSL Healthcare Inc. is recalling its Central Line Dressing Kit, Model/Catalog Number 2717H, due to the inclusion of Webcol Large Alcohol Prep Pads that were subsequently recalled for non-sterility. The affected product is identified by UDI-DI 00661392054738, Lot# 6A3181, with an expiration date of 11/30/2026.

Approximately 3,880 units of the Central Line Dressing Kit were distributed nationwide to locations in Maryland, Illinois, and Minnesota. The non-sterile prep pads pose a potential infection risk if used in medical procedures where sterility is required.

Patients and healthcare providers who have received or are using this dressing kit should stop use immediately. Healthcare facilities should contact LSL Healthcare Inc. for instructions regarding the return or proper handling of affected units. Anyone with questions about this recall should contact the recalling firm or the FDA.

The recalled product

Product
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2717H
Manufacturer
LSL Healthcare Inc.
Category
Medical Device — Wound care / Central line supplies
Hazard
Affected units
3,880

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. 2717H
  • UDI-DI 00661392054738
  • Lot# 6A3181
  • Expiration Date 11/30/2026 GTIN: (01)00661392054738(10)6A3181(17)261130

Distribution

Distributed nationwide across the United States.

The notice also names 3 states specifically:

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.

See all 6 products in this recall →

Related recalls

Same manufacturer · LSL Healthcare Inc.

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Same hazard · non sterility

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