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
ReasonBD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.
ProductLSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit
Quantity1400 kits
DistributionUS Nationwide distribution in the state of Idaho.
Initiated2025-12-22
Classified2026-01-29
Recall numberZ-1219-2026
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-1219-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98245/

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