Mega Diagnostics Mega Diagnostics Ammonia/Alcohol Controls (Cat.# A7504-CTL) packaged in 5ml vials Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Mega Diagnostics Ammonia/Alcohol Controls (Cat.# A7504-CTL) packaged in 5ml vials
Brand
Mega Diagnostics
Lot Codes / Batch Numbers
Lot# 522202
Products Sold
Lot# 522202
Mega Diagnostics is recalling Mega Diagnostics Ammonia/Alcohol Controls (Cat.# A7504-CTL) packaged in 5ml vials due to Potential for microorganism growth in the alcohol standard and or unexpected QC changes in the Ammonia portion of the Ammonia/Alcohol control product.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for microorganism growth in the alcohol standard and or unexpected QC changes in the Ammonia portion of the Ammonia/Alcohol control product.
Recommended Action
Per FDA guidance
The firm sent a recall notification to their customer in Indonesia and advised them to dispose of the product
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