LSL Healthcare recalls IV Start Kit Model 3131 due to non-sterile alcohol prep pads that could cause infections during medical procedures. Affected units have specific lot codes and expiration dates.
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
LSL Healthcare is recalling its IV Start Kit Model 3131 because the alcohol prep pads inside are not sterile. This poses a risk of infection during medical procedures if the kit is used without proper sterilization.
The alcohol prep pads in the kit are not sterile, which means they could introduce harmful bacteria during medical procedures. This risk is specific to situations where the pads are used for cleaning skin before injections or IV starts.
Healthcare professionals using the IV Start Kit Model 3131 are most at risk. Patients receiving medical procedures with this kit could be affected if the non-sterile pads are used.
Check for the model number 3131 on the kit. The lot code is 6A3139 with an expiration date of January 21, 2028. The kit may also have a UDI-DI code 00661392054271.
Look for the model number 3131, lot code 6A3139, and expiration date of January 21, 2028 on the IV Start Kit.
The alcohol prep pads in the IV Start Kit Model 3131 are not sterile, which could lead to infections during medical procedures.
Check for the model number 3131, lot code 6A3139, and expiration date of January 21, 2028 on the kit.
The recall record does not specify a remedy, so contact LSL Healthcare directly for guidance.
We’ve drafted a message you can send LSL Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1932-2026 — LSL Healthcare LSL Healthcare Hello, I own a LSL Healthcare that is covered by recall Z-1932-2026 from LSL Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
