The Recall Desk
HighFDA (Devices)·Z-1929-2026·Announced 2026-04-29

LSL Healthcare Central Line Dressing Change Kit Recalled for Non-Sterility

LSL Healthcare is recalling its Standard Central Line Dressing Change Kit (Model 2717J) because the included Webcol Large Alcohol Prep Pads were found to be non-sterile.

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 of a medical device where non-sterility poses a risk of harm in a high-risk procedure (central line care). The source explicitly classifies this as Class II and describes a sterility defect in a critical-use medical product, meeting the rubric criterion for High severity when no reported illnesses are documented.

Plain-English summary

LSL Healthcare Inc. is recalling 3,460 units of the Standard Central Line Dressing Change Kit, Model/Catalog Number 2717J, distributed nationwide in Maryland, Illinois, and Minnesota. The kits contain Webcol Large Alcohol Prep Pads that were subsequently found to be non-sterile.

Central line dressing change kits are medical procedure kits used in healthcare settings. The non-sterility of the included alcohol prep pads may compromise the sterile field required for safe central line care procedures.

Affected lot numbers include 6A3043 (expiration 11/30/2026) and 6B3076 (expiration 01/31/2027). Consumers and healthcare facilities with affected kits should stop using them immediately and contact LSL Healthcare Inc. or consult with their medical director regarding appropriate next steps.

The recalled product

Product
LSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J
Manufacturer
LSL Healthcare Inc.
Category
Medical Device — Dressing Change Kit / Central Line
Hazard
Affected units
3,460

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. 2717J
  • UDI-DI 00661392054721
  • Lot# 6A3043
  • Expiration Date 11/30/2026. Lot#6B3076

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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