Ameditech Inc: Medical Device Recall in 2015 - (Recall #: Z-0501-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

EDI BZO Uncut Sheet - Cup*, Item No. 160170

Product Classification:

Class III

Date Initiated: November 16, 2015

Date Posted: December 30, 2015

Recall Number: Z-0501-2016

Event ID: 72651

Reason for Recall:

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 particular BZO compounds for which there may be reduced reactivity are Clonazepam and Chlordiazepoxide.

Status: Terminated

Product Quantity: 45,584 kits

Code Information:

141260 141294 141909 141925 142074 142243 142428 142614 142712 142911 144555 151925 152003 152223 152498 152723 152897 153311 153559 153818 154184 152103

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated