THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU
Reported: December 30, 2015 Initiated: November 16, 2015 #Z-0542-2016
Product Description
THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU
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.
Details
- Recalling Firm
- Ameditech Inc
- Units Affected
- 100 kits
- Distribution
- Nationwide Distribution.
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
THERMO FISHER 8 DRUG CASSETTE, Item No. MTPA-8MBAU. Recalled by Ameditech Inc. Units affected: 100 kits.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 30, 2015. Severity: Low. Recall number: Z-0542-2016.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11