Product Recalls in Connecticut

Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,587 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,587 in last 12 months

Showing 1112111140 of 28,245 recalls

Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: ProScreen" Drugs of Abuse Test (AMT Item/ AMT Description): PSD-6MB/...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: First Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC) Recalled...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Alere iScreen Single Drug Detection (AMT Item Number/ AMT Description):...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Alere iScreen Multi Drug Detection (AMT Item Number/ AMT Description):...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: MicroTox (AMT Item Number/ AMT Description): MTPA-6MBAU / "MicroTox...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Oratect III Oral Fluid Drug Screen Device (AMT Item Number/ Recalled by...

The Issue: XXX

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Alere iCup Drug Detection (AMT Item Number/ AMT Description): I-DXA-10/...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: Fastect¿ II Drug Screen Dipstick Test Single Drug Detection (AMT Recalled by...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: First Check 1 Panel Drug Cup: (THC) Recalled by Ameditech Inc Due to Various...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2020· Ameditech Inc

Recalled Item: CLIA Waived Rapid Drug Test (AMT Item Number/ AMT Description): Recalled by...

The Issue: Various immunoassay enzymes failed product performance, thereby the products...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2020· ArthroCare Corporation

Recalled Item: Speed Stitch Needle Cassette Recalled by ArthroCare Corporation Due to Due...

The Issue: Due to a supplier error where a portion of the raw material was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2020· GE Healthcare, LLC

Recalled Item: NM/CT 850 Model Number: H3907AD Recalled by GE Healthcare, LLC Due to Rotor...

The Issue: Rotor bearing screws were found loose on detector.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2020· GE Healthcare, LLC

Recalled Item: Discovery NM 630 Model # H3101RH Recalled by GE Healthcare, LLC Due to Rotor...

The Issue: Rotor bearing screws were found loose on detector.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2020· GE Healthcare, LLC

Recalled Item: NM/CT 870 DR Model # H3100AS Recalled by GE Healthcare, LLC Due to Rotor...

The Issue: Rotor bearing screws were found loose on detector.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2020· GE Healthcare, LLC

Recalled Item: Discovery NM670 Pro Model # H3100XB Recalled by GE Healthcare, LLC Due to...

The Issue: Rotor bearing screws were found loose on detector.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2020· GE Healthcare, LLC

Recalled Item: NM/CT 870 CZT Model # H3906CW Recalled by GE Healthcare, LLC Due to Rotor...

The Issue: Rotor bearing screws were found loose on detector.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2020· GE Healthcare, LLC

Recalled Item: NM 830 Model # H3910AC Recalled by GE Healthcare, LLC Due to Rotor bearing...

The Issue: Rotor bearing screws were found loose on detector.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2020· GE Healthcare, LLC

Recalled Item: Discovery 670 DR Model # H3100BT Recalled by GE Healthcare, LLC Due to Rotor...

The Issue: Rotor bearing screws were found loose on detector.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2020· GE Healthcare, LLC

Recalled Item: NM/CT 860 Recalled by GE Healthcare, LLC Due to Rotor bearing screws were...

The Issue: Rotor bearing screws were found loose on detector.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing