Facility

LSL HEALTHCARE

2 recall(s) on record — most severe on record: Class II.

Key facts

2recalls · worst Class II

1inspections · worst NAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	1420054
Establishment type	Repack or Relabel Medical Device
Location	6200 W Howard St Niles, IL, US 60714
Registration status	Active · expires 2026
Parent company	LSL Healthcare (owner-operator 1420054)
Brand names	LSL Polymer Patient Examination Glove

Activity by year

Recalls (2)
Inspections (1)

Devices registered here (1)

Polymer Patient Examination Glove
Product code LZA (opens in a new tab) · Class I · General Hospital · 21 CFR 880.6250

Recalls & enforcement

Class IIOngoing2026-03-09
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Class IIOngoing2025-12-22
BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.

FDA inspections (1)

NAI2016-10-25
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by LSL Healthcare

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

Cite this record

RegWarden. “LSL HEALTHCARE (FEI 1420054) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1420054-lsl-healthcare/

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