Radiometer America Inc SafeClinitubes, REF 942-892, D957P-70-100x1, contained in kits containing 250 SafeClinitubes, insert, mixing wires and end caps. Capillary samplers for drawing small amounts of blood for blood gas analysis. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SafeClinitubes, REF 942-892, D957P-70-100x1, contained in kits containing 250 SafeClinitubes, insert, mixing wires and end caps. Capillary samplers for drawing small amounts of blood for blood gas analysis.
Brand
Radiometer America Inc
Lot Codes / Batch Numbers
Lot R0043, exp. 01/2008, R0044, exp. 01/2008, and R0045, exp. 03/2008.
Products Sold
Lot R0043, exp. 01/2008; R0044, exp. 01/2008; and R0045, exp. 03/2008.
Radiometer America Inc is recalling SafeClinitubes, REF 942-892, D957P-70-100x1, contained in kits containing 250 SafeClinitubes, insert due to The clinitubes are not able to be filled due to contamination with silicone during production.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The clinitubes are not able to be filled due to contamination with silicone during production.
Recommended Action
Per FDA guidance
The firm notified their customers of this recall with a letter dated 6/22/2006. The letter informs the customers of the problem with the affected lots of SafeCLINITUBES and asks that the customers discard any remaining boxes of affected product on-site. The recall letter is accompanied by a FAX FORM (response form) which the customer is asked to complete in order to request replacement product to be sent to their individual locations.
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