CLASS II ONGOING Device recall · Reported 29 Apr 2026 · FDA Enforcement Report

Standard Central Line Dressing Change Kit recalled by LSL Healthcare

LSL Healthcare is recalling Standard Central Line Dressing Change Kit, distributed nationwide in the US. The recall was initiated on 9 Mar 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: Model No. 2717J; UDI-DI 00661392054721; Lot# 6A3043, Expiration Date 11/30/2026. Lot#6B3076, Expiration Date 01/31/2027 GTIN: (01)00661392054721(10)6A3043(17)261130 GTIN: (01)00661392054721(10)6B3076(17)260131
Quantity recalled3460 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1929-2026
FDA event ID
98631
Recalling firm
LSL Healthcare, Niles, IL
Classification
Class II
Status
Ongoing
Recall initiated
9 Mar 2026
FDA classified
22 Apr 2026
Reported
29 Apr 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Sterility

Timeline

9 Mar 2026Recall initiated by company
22 Apr 2026Classified by FDA+44 days
29 Apr 2026Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

LSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J

Where it was distributed

US Nationwide distribution in the states of MD, IL, MN.

Nationwide IllinoisMarylandMinnesota

Questions about this recall

Why was it recalled?

Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.

Which lots are affected?

Lot Code: Model No. 2717J; UDI-DI 00661392054721; Lot# 6A3043, Expiration Date 11/30/2026. Lot#6B3076, Expiration Date 01/31/2027 GTIN: (01)00661392054721(10)6A3043(17)261130 GTIN: (01)00661392054721(10)6B3076(17)260131

Where was it sold?

US Nationwide distribution in the states of MD, IL, MN.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

5 other products · FDA event 98631

This product is part of a recall event; the main page for the event is Wound Closure Tray recalled by LSL Healthcare.

ReportedClassRecallCompanyReasonWhere
CLASS IIWound Closure Tray recalled by LSL HealthcareLSL HealthcareSterilityNationwide
CLASS IIFoley Urine Collection Kit recalled by LSL HealthcareLSL HealthcareSterilityNationwide
CLASS IICentral Line Dressing Kit recalled by LSL HealthcareLSL HealthcareSterilityNationwide
CLASS IIIV Start Kit recalled by LSL HealthcareLSL HealthcareSterilityNationwide
CLASS IIInfant Central Line Dressing Change Kit recalled by LSL HealthcareLSL HealthcareSterilityNationwide

More recalls from LSL Healthcare

All 7
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIInfant Central Line Dressing Change Kit recalled by LSL HealthcareLSL HealthcareSterilityNationwide
DeviceCLASS IIIV Start Kit recalled by LSL HealthcareLSL HealthcareSterilityNationwide
DeviceCLASS IICentral Line Dressing Kit recalled by LSL HealthcareLSL HealthcareSterilityNationwide
DeviceCLASS IIFoley Urine Collection Kit recalled by LSL HealthcareLSL HealthcareSterilityNationwide
DeviceCLASS IIWound Closure Tray recalled by LSL HealthcareLSL HealthcareSterilityNationwide

Other Other Medical Devices recalls

All 13,778
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IICitric Complete Dry Citric Acid Concentrate recalledNipro Renal Soultions USAOtherNationwide
DeviceCLASS IKit: Epidural/Pain TQC 20/Cs recalled by Medical Action IndustriesMedical Action Industries Inc. 306Sterility6 states
DeviceCLASS IIHalyard IV Start Kit Non-Sterile recalled by Avid MedicalAvid MedicalSterilityNationwide
DeviceCLASS IKit: Single Shot Epidural 20/Cs recalled by Medical Action IndustriesMedical Action Industries Inc. 306Sterility6 states
DeviceCLASS IIAMS Convenience Kit: Dsaek Pack - RX recalledWindstone Medical PackagingDevice MalfunctionNationwide