Life Technologies recalls Gibco DPBS calcium and magnesium bottles due to leaky caps that compromise sterility. Affected units sold with SKU 14040141, lot 1994520, expiring June 2021.
Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
Life Technologies recalls Gibco DPBS calcium and magnesium bottles because the bottle caps can leak, making the products unsafe for lab use. This could lead to contamination of samples if the bottles are not properly sealed.
The bottle caps have a defect that causes leaks, which compromises the sterility of the product. This means the solutions could become contaminated if the bottles are not properly sealed, leading to inaccurate lab results or unsafe conditions.
Lab users and researchers who own or use Gibco DPBS calcium and magnesium bottles with SKU 14040141, lot 1994520, expiring June 2021 are most at risk. The hazard affects products used in in-vitro diagnostic settings.
Check for the SKU 14040141 label on the bottle, and the lot number 1994520 with an expiration date of June 30, 2021. The product is for in-vitro diagnostic use only.
Inspect the bottle cap for leaks or signs of damage that could compromise sterility.
The bottle caps have a defect that causes leaks, compromising the sterility of the product for in-vitro diagnostic use.
The recall record does not specify a remedy, so check the bottle cap for leaks and consider discarding if it appears damaged.
The product is not safe for use if the bottle cap leaks, as it can compromise sterility and lead to contamination.
We’ve drafted a message you can send Life Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0172-2019 — Life Technologies Life Technologies Hello, I own a Life Technologies that is covered by recall Z-0172-2019 from Life Technologies. 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.
