CLASS II ONGOING Device recall · Reported 29 Apr 2026 · FDA Enforcement Report
Infant Central Line Dressing Change Kit recalled by LSL Healthcare
LSL Healthcare is recalling Infant Central Line Dressing Change Kit, distributed nationwide in the US. The recall was initiated on 9 Mar 2026 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1931-2026
- FDA event ID
- 98631
- Recalling firm
- LSL Healthcare, Niles, IL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 9 Mar 2026
- FDA classified
- 22 Apr 2026
- Reported
- 29 Apr 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Sterility
- Device type
- Other Medical Devices
Timeline
| 9 Mar 2026 | Recall initiated by company | |
| 22 Apr 2026 | Classified by FDA | +44 days |
| 29 Apr 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
LSL Healthcare, Infant Central Line Dressing Change Kit, Model/Catalog Number: 2925H
Where it was distributed
US Nationwide distribution in the states of MD, IL, MN.
Questions about this recall
Why was it recalled?
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
Which lots are affected?
Lot Code: Model No. 2925H; UDI-DI 00661392052635; Lot#6B3022, Expiration Date 11/30/2026 GTIN: (01)00661392052635(10)6B3022(17)261130
Where was it sold?
US Nationwide distribution in the states of MD, IL, MN.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
5 other products · FDA event 98631This product is part of a recall event; the main page for the event is Wound Closure Tray recalled by LSL Healthcare.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Wound Closure Tray recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide | |
| CLASS II | Foley Urine Collection Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide | |
| CLASS II | Standard Central Line Dressing Change Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide | |
| CLASS II | Central Line Dressing Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide | |
| CLASS II | IV Start Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
More recalls from LSL Healthcare
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | IV Start Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | Central Line Dressing Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | Standard Central Line Dressing Change Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | Foley Urine Collection Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | Wound Closure Tray recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
Other Other Medical Devices recalls
All 13,778| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Citric Complete Dry Citric Acid Concentrate recalled | Nipro Renal Soultions USA | Other | Nationwide |
| Device | CLASS I | Kit: Epidural/Pain TQC 20/Cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Sterility | 6 states |
| Device | CLASS II | Halyard IV Start Kit Non-Sterile recalled by Avid Medical | Avid Medical | Sterility | Nationwide |
| Device | CLASS I | Kit: Single Shot Epidural 20/Cs recalled by Medical Action Industries | Medical Action Industries Inc. 306 | Sterility | 6 states |
| Device | CLASS II | AMS Convenience Kit: Dsaek Pack - RX recalled | Windstone Medical Packaging | Device Malfunction | Nationwide |