Roche Diagnostics Corp. ACCU-CHEK Inform base unit; catalog no. 3035131. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ACCU-CHEK Inform base unit; catalog no. 3035131.
Brand
Roche Diagnostics Corp.
Lot Codes / Batch Numbers
All units.
Products Sold
All units.
Roche Diagnostics Corp. is recalling ACCU-CHEK Inform base unit; catalog no. 3035131. due to Exposure to excessive disinfectant or cleaning solution may cause overheating, melting, or smoke.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Exposure to excessive disinfectant or cleaning solution may cause overheating, melting, or smoke.
Recommended Action
Per FDA guidance
A recall notice dated 6/30/04 was sent to each customer instructing them on proper cleaning methods, asking them to inspect their units for damage, and providing warning stickers for attachment to the base units.
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