Terumo Bct, Inc..
10811 W COLLINS AVE, Lakewood, CO, US
Registered product codes
12 product codes
Recent MDR events
64 on file
- SPECTRA OPTIAJun 8, 2026Malfunction25426378
- SPECTRA OPTIAMar 30, 2026Malfunction24709674
- SPECTRA OPTIA IDL SETFeb 12, 2026Malfunction24321234
- SPECTRA OPTIA®Sep 4, 2025Malfunction22962993
- COBE BLOOD CELL PROCESSING SETJan 21, 2025InjuryMW5164928
- SPECTRA OPTIANov 4, 2024InjuryMW5162142
- SPECTRA OPTIASep 23, 2024Malfunction20278455
- SPECTRA OPTIA IDL SETAug 13, 2024Malfunction19972023
- SPECTRA OPTIA®Jul 8, 2024Malfunction19688862
- SPECTRA OPTIA®Jul 2, 2024Malfunction19654349
Recalls
4 on file
- TerminatedNov 30, 2016
Terumo BCT announces a voluntary field action for the Harvest : Adiprep Adipose Transfer System because the affected product is incorrectly labeled and has the potential for operator confusion.
View FDA record ↗ - TerminatedUnknown
Certain lots of the Harvest Graft Delivery System GDP-10 Procedure Packs may have a lack of a seal on the inner pouch.
View FDA record ↗ - TerminatedUnknown
The patient labels included in the BMAC system procedure packs, catalog numbers 51416 and 51423, are printed with an incorrect lot number, catalog number, and expiry date; the lot number on the procedure pack box label is correct. The expiration noted was not beyond initiation date of the recall. Since the product is noted as sterile, the clearance for K103340, K052925 and K991430 raises question if product was cleared with a sterility claim. Further post-market follow-up will be required to assess the safety risk of the product.
View FDA record ↗ - TerminatedUnknown
The patient labels included in the BMAC system procedure packs, catalog numbers 51416 and 51423, are printed with an incorrect lot number, catalog number, and expiry date; the lot number on the procedure pack box label is correct. The expiration noted was not beyond initiation date of the recall. Since the product is noted as sterile, the clearance for K103340, K052925 and K991430 raises question if product was cleared with a sterility claim. Further post-market follow-up will be required to assess the safety risk of the product.
View FDA record ↗
Compliance history
Matched by FEI 1000117351.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.