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DMEM (Dulbecco's Modified Eagle Medium)

LIFE TECHNOLOGIES CORPORATION · Model 11995115 · UDI-DI 10190302002165

NDS
9
510(k) clearances
0
Adverse events
7
Recalls
1
Facilities

Recalls

DateFirmReason
2019-06-11Life Technologies CorporationComponent was not tested by the supplier for adventitious agents
2018-05-10Life Technologies, Corp.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 pac
2018-05-10Life Technologies, Corp.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 pac
2018-05-10Life Technologies, Corp.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 pac
2018-05-10Life Technologies, Corp.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 pac
2018-05-10Life Technologies, Corp.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 pac
2018-05-10Life Technologies, Corp.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 pac

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.