Roche Diagnostics Corp. Roche/Hitachi K Electrode, a potassium electrode for use with the Roche/Hitachi models 717,747, 902, 911,912, 917, Modular and Cobas c 501clinical chemistry analyzers; Roche Catalog/Part Number 10825441001/ US # 722-4402. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Roche/Hitachi K Electrode, a potassium electrode for use with the Roche/Hitachi models 717,747, 902, 911,912, 917, Modular and Cobas c 501clinical chemistry analyzers; Roche Catalog/Part Number 10825441001/ US # 722-4402.
Brand
Roche Diagnostics Corp.
Lot Codes / Batch Numbers
Lots I90, I93 and I95 (alpha I and two digits)
Products Sold
Lots I90, I93 and I95 (alpha I and two digits)
Roche Diagnostics Corp. is recalling Roche/Hitachi K Electrode, a potassium electrode for use with the Roche/Hitachi models 717,747, 902, due to Expired product (dated 2006.06) was shipped as replacement for recalled product.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Expired product (dated 2006.06) was shipped as replacement for recalled product.
Recommended Action
Per FDA guidance
Consignees were notified by phone and sent a recall letter dated 7/21/06 via fax, which instructed them to discontinue use of these lots of product and to discard them.
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