Radiometer America Inc Capillary (end) caps, accessory for use with blood gas analyzers included in Radiometer''s CLINITUBES kits. The end caps are packaged in bags. These bags are placed in the capillary tube kit which also contains: capillary tubes, end caps, mixing wires, and a magnet. Each kit may contain 1 or 5 bags depending on the kit model. Each bag contains: 110 Green caps per bag and 160 Red caps per bag. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Capillary (end) caps, accessory for use with blood gas analyzers included in Radiometer''s CLINITUBES kits. The end caps are packaged in bags. These bags are placed in the capillary tube kit which also contains: capillary tubes, end caps, mixing wires, and a magnet. Each kit may contain 1 or 5 bags depending on the kit model. Each bag contains: 110 Green caps per bag and 160 Red caps per bag.
Brand
Radiometer America Inc
Lot Codes / Batch Numbers
Red Caps - Model #904-439 lot number less than 0535033
Products Sold
Red Caps - Model #904-439 lot number less than 0535033
Radiometer America Inc is recalling Capillary (end) caps, accessory for use with blood gas analyzers included in Radiometer''s CLINITUBE due to Capilliary end caps, an accessory for ABL blood gas analyzers, leak blood from capillary tubes during transport.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Capilliary end caps, an accessory for ABL blood gas analyzers, leak blood from capillary tubes during transport.
Recommended Action
Per FDA guidance
The firm notified their customers of this recall action with a letter dated 3/22/2006. The letter was accompanied by a single bag of new end caps. The letter informs the customers of the ''leakage'' problem and asks that the customer examine their inventories and discard any of the referenced end caps found on-hand at any of their various locations. The letter also includes a response form to be faxed back to Radiometer indicating the amount of replacement capillary end caps required by the customer in addition to the one bag received. The recalling firm also notified the customers that the suspect end caps will all be replaced ASAP.
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