FDA recall record

Life Technologies Gibco Sodium Pyruvate (100 mM) SKU 11360070, for In-Vitro Diagnostic Use recall — FDA Z-0173-2019

Leaky bottles due to a defect in the bottle cap compromising the sterility of the product

Class IIclassification
Z-0173-2019official record ID
Oct 24, 2018report date

Recall record at a glance

Official recordZ-0173-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLife Technologies, Corp.
Report dateOct 24, 2018
Recall initiation dateAug 24, 2018
Quantity41 units
LocationGrand Island, NY, United States

Official product description

Gibco Sodium Pyruvate (100 mM) SKU 11360070, for In-Vitro Diagnostic Use

Why the product was recalled

Leaky bottles due to a defect in the bottle cap compromising the sterility of the product

Distribution information

Nationwide: Foreign: Argentina Australia Canada China Great Britain Hong Kong India Japan Mexico Netherlands New Zealand Singapore South Korea Taiwan

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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