Product Recalls in Colorado

Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,133 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,133 in last 12 months

Showing 11261–11280 of 28,964 recalls

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: Henry Schein One Step + DOA Cup (AMT Item Number/ Recalled by Ameditech Inc...

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 14 Panel Drug Cup: (BMC style) Recalled by Ameditech Inc Due to...

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: TDDA Drugs of Abuse Cup(AMT Item/ AMT Description): TDDA-6MBAU-CUP /"TDDA...

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 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 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· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...

The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Clinical Innovations, LLC

Recalled Item: Clinical Innovations ROM Plus Collection Kit IFU: ROM Plus Rupture Recalled...

The Issue: Possible false negative or false positive results. The incorrect sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Sobel Westex

Recalled Item: SOBEL WESTEX Disposable Isolation Gown Made in China RN#71273 SBPP Recalled...

The Issue: Due to non-surgical isolation gowns not meeting all performance test...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Battelle Memorial Institute

Recalled Item: Critical Care Decontamination System (CCDS) Compatible N95 respirators -...

The Issue: Masks processed at one site were not maintained at levels of condensation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2020· Pharmaceutical Innovations, Inc.

Recalled Item: Ultra/Phonic Focus BP Conforming Gel Pads Recalled by Pharmaceutical...

The Issue: The firm registered the product as a Class I device, but has since been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit Recalled by Covidien, LP Due to...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2020· Covidien, LP

Recalled Item: Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm Recalled by...

The Issue: The device staples may not properly form upon application preventing...

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

Class II — Potential Health HazardOngoing