Overview of recall records associated with Life Technologies, Corp., including dates, categories and classifications where available.
Classification mix: Class II: 10.
Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
Leaky bottles due to a defect in the bottle cap compromising the sterility of the product
It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging…
It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging…
It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging…
It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging…
It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging…
It has been determined that the fill port tube seal integrity was compromised during the manufacture of the product lot. This may cause media to leak out of the primary sterile packaging…
This page summarizes recall records in which the official source identifies Life Technologies, Corp. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
