Cyto-Chex BCT 218980Recalls & reported problems
Streck, Inc. · A direct-draw blood collection tube for the preservation of whole blood specimens for immunophenotyping by flow cytometry. 2 ml vials. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Feb 23, 2017Class IIOpen, Classified
Complaints of the 2.0ml tube stopper coming loose during phlebotomy when small diameter tube adapters were not utilized. Such adapters aid with centering small diameter tubes to properly pierce the middle of the stoppers.
Z-1684-2017 · Root cause: Error in labeling · Recall details · FDA record ↗
Other Tubes, Vacuum Sample, With Anticoagulant devices
- Vacuette 454322Greiner Bio-One GmbH · Tubes, vacuum sample, with anticoagulant3 recalls0 reports
- BD MiniDraw™ H&H Capillary Blood Collection Tube 366603Becton, Dickinson And Company · Tubes, vacuum sample, with anticoagulant141 reports
- BD Vacutainer® K2 EDTA (K2E) Plus Blood Collection Tubes 366643Becton, Dickinson U.K. Limited · Tubes, vacuum sample, with anticoagulant124 reports
- Cyto-Chex BCT 213559Streck, Inc. · Tubes, Vacuum Sample, With Anticoagulant1 recall0 reports
- Vacuette 454332Greiner Bio-One GmbH · Tubes, vacuum sample, with anticoagulant1 recall0 reports
- Vacuette 454334Greiner Bio-One GmbH · Tubes, vacuum sample, with anticoagulant1 recall0 reports
- BD MiniDraw™ Finger Sleeve, Extra-Large 366616Becton, Dickinson And Company · Tubes, vacuum sample, with anticoagulant25 reports
- BD MiniDraw™ Finger Sleeve, Large 366615Becton, Dickinson And Company · Tubes, vacuum sample, with anticoagulant21 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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