Medline recalls nail kits with model POD14214 due to potential contamination in sterile saline wound wash. Affected units have specific lot numbers; stop using if you own one.
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
Medline is recalling nail kits with model number POD14214 because the sterile saline wound wash inside may not meet sterility standards. This could lead to infections if used improperly. The recall affects specific lot numbers and units sold between 2023 and 2024.
The sterile saline wound wash in these kits may not meet required sterility levels. This means the product could be contaminated, increasing the risk of infection if used on wounds or skin. The hazard is related to the manufacturing process, not normal use conditions.
People who own or use Medline nail kits with model number POD14214 are affected. Those using the kits for medical purposes, especially in healthcare settings, are at higher risk due to potential contamination.
Check for the model number POD14214 on the kit. Affected units have specific lot numbers: 25CBS147, 25CBJ329, 25ABU209, 24DBJ364, 24DBB718, 23JBV524, and 23IBU998.
Look for the model number POD14214 and the lot numbers listed above on the kit.
The sterile saline wound wash in these kits may not meet required sterility levels, which could lead to contamination and infection risk.
Check for the model number POD14214 and lot numbers: 25CBS147, 25CBJ329, 25ABU209, 24DBJ364, 24DBB718, 23JBV524, or 23IBU998.
The recall indicates a potential contamination risk, but the remedy is not specified. You should check if your kit is affected before deciding.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1432-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1432-2026 from Medline. 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.
