🔬

Diagnostic Equipment

🏥 Medical Devices 6,554 recalls

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Sterility of the product cannot be assured.

Oct 21, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

ProScreen 10 Drug Panel Cassette Test, Item No. CPSP-10PPX; ProScreen 10 Panel Cup, Item No. PSCup-10MMO-300, PSCup-10M, PSCupA-10MO, PSCUp-10AB; ProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM; ProScreen 10 Panel Dip Card, Item No. PSD-10MMO-300, PSD-10MOX, PSD-10M, PSD-10CMO3, PSD-10APO-300; ProScreen 10 Panel Dip Card w/Adult, Item No. PSDA-10MO, PSDA-10MMO-300; ProScreen 11 Panel Dip Card, Item No. PSD-11MT; ProScreen 12 Drug Cup w/Adulteration, Item No. PSCupA-12TBU; ProScreen 12 Panel Cup w/Adult., Item No. PSCupA-12M, PSCupA-12PP; ProScreen 12 Panel Dip Card, Item No. PSD-12BUP ProScreen 5 Panel Dip Card, Item No. PSD-5MB; ProScreen 5 Panel Dip Card w/Adult, Item No. PSDA-5MB-300; ProScreen 6 Panel Cassette w/Adult (AU), Item No. PSPA-6MBAU; ProScreen 6 Panel Cup w/Adult (AU), Item No. PSCupA-6MBAU; ProScreen 6 Panel Dip Card, Item No. PSD-6MBO, PSD-6MTDBO-300, PSD-6MB, PSD-6BUPO; ProScreen 7 Panel Dip Card, Item No. PSD-7MO, PSD-7M; ProScreen 8 Panel Dip Card, Item No. PSD-8P; ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P; ProScreen 9 Panel Dip Card, Item No. PSD-9P; ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W; ProScreen CLIA Waived Cup with 6 Drugs, Item No. PSCup-6BO-W; ProScreen CLIA Waived Cup with 8 Drug, Item No. PSCup-8P-W; ProScreen Cup, Item No. PSCup-6MB-W, PSCupA-6MB-W, PSCup-6BO-W, PSCup-8P-W, PSCUp-10AB, PSCup-10MMO-300; ProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-W; These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips, including Benzodiazepine (BZO). They are used to obtain a visual, qualitative result and are intended for professional and point of care use. ¿¿¿

Ameditech

Class I - Dangerous

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

When a Philips monitor/defibrillator is receiving an ECG signal from an auxiliary bedside monitor via a sync cable, the following can occur if the monitor/defibrillator experiences interference from electrical fast transients (EFTs) while connected to AC power: On the HeartStart MRx and HeartStart XL, EFT noise can be misinterpreted as an R-wave. On the HeartStart XL+, EFT noise can disable ECG monitoring, and potentially interrupt demand mode pacing.

Nov 19, 2014 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →