Data Foundry

Medical device recalls 2013

Vacuette Cellestis 1 ml QuantiFERON¿ TB ANTIGEN — Class II medical device recall Z-0889-2013

Terminated recall by Cellestis Inc, reported 2013-03-06, distributed nationwide. Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and HA TB Blood Collection Tubes due

Recall numberZ-0889-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCellestis Inc, Santa Clarita, CA, United States
Recall initiated2012-09-27
Classified2013-02-26
Reported by FDA2013-03-06
Terminated2013-04-25
DistributedNationwide (US)
Countries outside the USAR, AT, AU, BE, BG, CH, CZ, DE, DK, EE, FI, FR, GB, IE, IL, JO, LU, MX, NL, NZ, PE, PL, SA, SI, SK, TR, ZA
Quantity29,690 units
Lot numbersA111103M
Model numbers0592-0501, 454413, HE0396
Expiration dates2013-02-28

Product

Vacuette Cellestis 1 ml QuantiFERON¿ TB ANTIGEN (HA) High Altitude: Shake 10x; REF 454413. HE0396. greiner bio-one; 13x75 50pcs.,1200 pcs in total. Product Usage: QuantiFERON¿-TB Gold (QFT) is an in vitro diagnostic test using a peptide cocktail simulation ESAT-6, CFP-10 and TB7.7 (p4) proteins to stimulate cells in heparinized whole blood.

Reason for recall

Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and HA TB Blood Collection Tubes due to potential contamination.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0889-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.