FDA Device recall Z-2248-2020
safeCLINITUBES Blood Sampler;REF 942-898;D957P-70-70x1
- FDA Device
- Class II
- terminated
- Published 2020-06-10
On 2020-06-10 the FDA classified a Class II recall of safeCLINITUBES Blood Sampler;REF 942-898;D957P-70-70x1 by Radiometer Medical Aps, citing the SafeCLINITUBES blood sampler may have insufficient aspiration capabilities ultimately resulting in lost samples.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2248-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-03-17 |
| Published | 2020-06-10 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Radiometer Medical Aps |
| Distribution | AK, AL, AR, CA, CO, CT, FL, GA, IA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, SD, TN, TX, UT, VA, WA, WI |
Product
safeCLINITUBES Blood Sampler;REF 942-898;D957P-70-70x1
Reason
The SafeCLINITUBES blood sampler may have insufficient aspiration capabilities ultimately resulting in lost samples.
Identifiers
| code_info | Lot numbers: R1431 - R1495 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2248-2020%22
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