# FDA recall Z-2248-2020

> **Radiometer Medical ApS** · Class II · device recall initiated 2020-03-17.

## Product

safeCLINITUBES Blood Sampler;REF 942-898;D957P-70-70x1

## Reason for recall

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

## Distribution

U.S.: 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,  and WI.  OUS:  Australia (New Zealand), Austria, Brazil  Canada, China,  Czech Republic (Slovakia),  Denmark, Dubai (United Arab Emirates), Egypt, Finland, France, Germany, Hong Kong, Hungary, Iceland, India, Ireland, Italy, Japan, Kazakhstan, Lithuania, Malawi, Malaysia,  Mauritius, Netherlands (Belgium), Nicaragua,  Norway, Poland, Portugal, Russia, Saudi Arabia, Serbia, South Africa, Spain, Sweden, Switzerland, Turkey (Cyprus), and United Kingdom.

## Key facts

- **Recall number:** Z-2248-2020
- **Recalling firm:** Radiometer Medical ApS
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-17
- **Report date:** 2020-06-10
- **Termination date:** 2022-07-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bronshoj, N/A, Denmark

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2248-2020

## Citation

> AI Analytics. FDA recall Z-2248-2020. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2248-2020. Source: US FDA. Licensed CC0.

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