Home › LIFE TECHNOLOGIES CORPORATION › STEMPROÒ MSC SFM Basal Medium CTS™
STEMPROÒ MSC SFM Basal Medium CTS™
LIFE TECHNOLOGIES CORPORATION · Model A1033401 · UDI-DI 10190302005166
NDS
Prescription
9
510(k) clearances
0
Adverse events
7
Recalls
1
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-06-11 | Life Technologies Corporation | Component was not tested by the supplier for adventitious agents |
| 2018-05-10 | Life 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 |
| 2018-05-10 | Life 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 |
| 2018-05-10 | Life 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 |
| 2018-05-10 | Life 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 |
| 2018-05-10 | Life 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 |
| 2018-05-10 | Life 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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Get your free API keyRead the docsData 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.