- Recalling firm
- LSL Healthcare Inc.
- Reason for recall
- Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
- Affected products (lot / model / serial)
- Lot Code: Model No. 3131; UDI-DI 00661392054271; Lot#6A3139, Expiration Date 01/21/2028 GTIN: (01)00661392054271(10)6A3139(17)280121
- Units affected
- 2200 units
- Distribution pattern
- US Nationwide distribution in the states of MD, IL, MN.
- Firm location
- Niles, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1932-2026
- Recall initiated
- March 9, 2026
- FDA classification date
- April 22, 2026
- FDA report date
- April 29, 2026
- FDA event ID
- 98631
- Last updated on HTM Vibe
- July 24, 2026