Recall Z-1115-2022

Radiometer Medical ApS · initiated April 8, 2022

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

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

Codes / lots: "All Lots" UDI/DI: 05700699565525

Reason for recall

Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf life of the product.

FDA-determined cause: Package design/selection

Action taken

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

Details

Recall number
Z-1115-2022
Initiated
April 8, 2022
Product code
JKA – Tubes, Vials, Systems, Serum Separators, Blood Collection
Quantity
7,228 boxes (100 units per box)
Distribution
Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, DC, FL, GA, IL, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NM, NY, OH, OK, OR, PA, TN, TX, WA, WI and the countries of Canada, Italy, Norway, Austria, Algeria, Argentina, Bolivia, Bosnia, Brazil, Burkina, Faso, Chile, Colombia, Cyprus, Ecuador, Egypt, Eswatin, Ethiopia, Greece, Guatemala, Israel, Lebanon, Libya…
Recalling firm
Radiometer Medical ApS, Bronshoj

Official FDA recall record