Life Technologies, Corp. recalls Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061
- Recall date
- August 24, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0174-2019
- FDA classification
- Class II
- Brand / firm
- Life Technologies, Corp.
- Sold / distributed
- Nationwide: Foreign: Argentina Australia Canada China Great Britain Hong Kong India Japan Mexico Netherlands New Zealand Singapore South Korea Taiwan
Why it was recalled
Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061
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