Home/Recalls/FDA-Z-1932-2026
FDA DevicesClass II

LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131

Published: April 29, 2026Recall ID: Z-1932-2026Category: devicesCountry: US

Reason for Recall / Hazard

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

Product Description & Identification

LSL Healthcare, IV Start Kit, Model/Catalog Number: 3131

Additional Source Details

FieldValue
CityNiles
StateIL
Event id98631
Address 16200 W Howard St
Address 2N/A
Code infoLot Code: Model No. 3131; UDI-DI 00661392054271; Lot#6A3139, Expiration Date 01/21/2028 GTIN: (01)00661392054271(10)6A3139(17)280121
Postal code60714-3404
Report date20260429
Product typeDevices
Product quantity2200 units
Reason for recallMedical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260309
Initial firm notificationE-Mail
Center classification date20260422

Overview

  • Recalling FirmLSL Healthcare Inc.
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution in the states of MD, IL, MN.
Official Agency Alert