Radiometer Medical ApS Akandevej 21 Bronshoj Denmark Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for injection. , IVD, Rx Only, Sterile EO, CE Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for injection. , IVD, Rx Only, Sterile EO, CE
Brand
Radiometer Medical ApS Akandevej 21 Bronshoj Denmark
Lot Codes / Batch Numbers
"All Lots" UDI/DI: 05700699565525
Products Sold
"All Lots" UDI/DI: 05700699565525
Radiometer Medical ApS Akandevej 21 Bronshoj Denmark is recalling Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin due to Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf life of the product.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf life of the product.
Recommended Action
Per FDA guidance
On April 26, 2022 Radiometer issued a "Urgent Medical Device Recall" notification via Email. The firm ask consignees to take the following actions: Radiometer kindly request you to stop using the affected product with immediate effect. To ensure patient safety in your facility, kindly follow the steps below: " Check your inventory of the above PICO50 Arterial Blood Samplers " Check for the above PICO50 Arterial Blood Samplers distributed in your institution. " Collect any of the above PICO50 Arterial Blood Samplers and put on quarantine " Complete the Recall Response Form (last page of this letter) and return to your Radiometer representative together with the quarantined PICO50 Arterial Blood Samplers. To ensure you receive credit for the PICO50 Arterial Blood Samplers, please contact Customer Service @ CSRsupport@radiometeramerica.com to receive a Return Goods Authorization
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026