Home / Recalls / Ameditech Inc / Z-3051-2020

Z-3051-2020 Class II Terminated

Recalled by Ameditech Inc — San Diego, CA

FDA device recall Z-3051-2020 was initiated by Ameditech Inc on August 18, 2020 and is designated Class II. Reason for recall: Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling. The recall status is terminated (terminated September 30, 2024). Affected quantity: 3600 units.

Recall Details

Product Type
Devices
Report Date
October 7, 2020
Initiation Date
August 18, 2020
Termination Date
September 30, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
3600 units

Product Description

Drug Screening Component: Uncut Sheets Part Number/ Description/ LOT Number 100163/ EDI OPI (300) Uncut Sheet-Card /187876, 100195/ EDI PPX Uncut Sheet-Card/ 187877, 160130/ EDI COC Uncut Sheet-Cup/ 188168, 160180/ EDI PCP Uncut Sheet-Cup/ 189027, 160140/ EDI THC Uncut Sheet Cup /189028, 160170/ EDI BZO Uncut Sheet-Cup/ 189081, 160120/ EDI MET1000 Uncut Sheet-Cup/ 189082, 160160/ EDI OPI2000 Uncut Sheet-Cup / 189123, 160130/ EDI COC Uncut Sheet-Cup/ 189124, 160160/ EDI OPI2000 Uncut Sheet-Cup/ 189166, 160163/ EDI OPI (300) Uncut Sheet-Cup/ 189191, 160110/ EDI AMP Uncut Sheet-Cup/ 189371, 160140/ EDI THC Uncut Sheet Cup/ 189372, 160123/ EDI MET(300) Uncut Sheet-Cup/ 189425, 160170/ EDI BZO Uncut Sheet-Cup/ 189426, 100163/ EDI OPI (300) Uncut Sheet-Card/ 189456, 160170/ EDI BZO Uncut Sheet-Cup/ 189565, 160180/ EDI PCP Uncut Sheet-Cup/ 189601, 160125/ EDI MET(500) Uncut Sheet-Cup/ 189748, 160130/ EDI COC Uncut Sheet-Cup/ 189786, 160160/ EDI OPI2000 Uncut Sheet-Cup / 189844, 160180/ EDI PCP Uncut Sheet-Cup/ 189937, 160172/ EDI BZO(200) Uncut Sheet-CUP/189956 Updated 09/03/2020: EDI Affected products -Catalog Numbers/ Lot Numbers 31105-3/ PI-01081 60503s-3ZC/ PH-10132 60600/ PH-11005

Reason for Recall

Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.

Distribution Pattern

US - Nationwide OUS - Australia, France, Germany, New Zealand, Singapore and Spain

Code Information

ALL Lots Within Expiry

Other recalls by Ameditech Inc

  • Z-3037-2020 Class II — MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen AMP30 (August 18, 2020)
  • Z-3046-2020 Class II — First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B (August 18, 2020)
  • Z-3032-2020 Class II — CLIA Waived Rapid Drug Test (AMT Item Number/ AMT Description): X07-CLIA-SDD (August 18, 2020)
  • Z-3029-2020 Class II — Alere iScreen Single Drug Detection (AMT Item Number/ AMT Description): X11-IS (August 18, 2020)
  • Z-3049-2020 Class II — First Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC); AMT Item Numb (August 18, 2020)
  • Z-3042-2020 Class II — ProScreen" Drugs of Abuse Test (AMT Item/ AMT Description): PSD-6MB/ "ProScre (August 18, 2020)
  • Z-3036-2020 Class II — ImmuTest Drugs of Abuse Cup (AMT Item Number/ AMT Description): IMCA-5AB-W / (August 18, 2020)
  • Z-3033-2020 Class II — Consult Diagnostics Drugs Abuse Test Cup (AMT Item Number/ AMT Description): (August 18, 2020)
  • Z-3047-2020 Class II — First Check 14 Panel Drug Cup: (BMC style); AMT Item Number 990700B (August 18, 2020)
  • Z-3039-2020 Class II — Noble 1 Step+ Cup (AMT Item Number/ AMT Description): NBCA-13A-B /"Noble 1 St (August 18, 2020)

FDA data resources