Radiometer America Inc Model #842-326 (pump tube for waste) & Model #842-327 (pump tube for solution), Waste Tubing used on ABL 7xx and ABL8xx, component of the ABL700/800 Blood Gas Analyzers, also included in service kits part no. 905-671 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Model #842-326 (pump tube for waste) & Model #842-327 (pump tube for solution), Waste Tubing used on ABL 7xx and ABL8xx, component of the ABL700/800 Blood Gas Analyzers, also included in service kits part no. 905-671
Brand
Radiometer America Inc
Lot Codes / Batch Numbers
Model #842-326 & Model #842-327, no lot numbers supplied.
Products Sold
Model #842-326 & Model #842-327, no lot numbers supplied.
Radiometer America Inc is recalling Model #842-326 (pump tube for waste) & Model #842-327 (pump tube for solution), Waste Tubing used o due to An increased failure rate was observed with the yellow rubber tubing. The tubing was found to be leaking blood and solutions after distribution.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
An increased failure rate was observed with the yellow rubber tubing. The tubing was found to be leaking blood and solutions after distribution.
Recommended Action
Per FDA guidance
The recalling firm issued a letter to their customers dated 5/22/2006. The letter informs the customer(s) of the tubing defect and provides the customer with one (1) tubing to deal with any immediate needs which they may have. Should the customer require additional waste pump tubing replacements, the letter is accompanied by a FAX FORM which can be used to request any amount of additional replacement tubing required. The letter also shows tthe address to which the replacement tubing is to be delivered, and provides a Purchase Order request to be used, if required.
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