Data Foundry

Medical device recalls 2020

safeCLINITUBES Blood Sampler — Class II medical device recall Z-2249-2020

Terminated recall by Radiometer Medical ApS, reported 2020-06-10, distributed in AK, AL, AR, CA, CO, CT, FL, GA…. The SafeCLINITUBES blood sampler may have insufficient aspiration capabilities ultimately resulting in lost sa

Recall numberZ-2249-2020
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmRadiometer Medical ApS, Bronshoj, N/A, Denmark
Recall initiated2020-03-17
Classified2020-06-02
Reported by FDA2020-06-10
Terminated2022-07-28
DistributedAK, 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
Countries outside the USAE, AT, AU, BE, BR, CA, CH, CN, CY, CZ, DE, DK, EG, ES, FI, FR, GB, HK, HU, IE, IN, IS, IT, JP, LT, MY, NI, NL, NO, NZ, PL, PT, RS, RU, SA, SE, SK, TR, ZA
Quantity5 units
Lot numbersR0291, R0301
Model numbers942-969

Product

safeCLINITUBES Blood Sampler;REF 942-969;D957P-70-45x1

Reason for recall

The SafeCLINITUBES blood sampler may have insufficient aspiration capabilities ultimately resulting in lost samples.

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-2249-2020. 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.