Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5

Recall Insight

This FDA Devices action (record #Z-0507-2016) was formally reported on December 30, 2015, with the manufacturer initiating the action on November 16, 2015. It is classified under Low severity (Class III), with a current status of Terminated. Ameditech Inc is listed as the recalling firm, operating out of San Diego, CA. Federal records indicate 320 kits units are affected.

The documented reason for this recall is: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity for up to two (2) of the nineteen (19) Benzodiazepine (BZO) compounds for which specificity information is provided in the product insert. The p… Distribution data in the federal record shows the product reached: Nationwide Distribution.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 11 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.