RegWardenFDA facility compliance records
Recall

Class II — LSL Healthcare Inc.

Recalling firmLSL Healthcare
Registered facilityLSL HEALTHCARE (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonMedical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
ProductLSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J
Quantity3460 units
DistributionUS Nationwide distribution in the states of MD, IL, MN.
Initiated2026-03-09
Classified2026-04-22
Recall numberZ-1929-2026
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — LSL Healthcare Inc. (Z-1929-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98631/

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