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. 2,563 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,563 in last 12 months

Showing 1814118160 of 51,434 recalls

DrugAugust 7, 2020· Open Book Extracts

Recalled Item: Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count NDC...

The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2020· Open Book Extracts

Recalled Item: Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ Recalled by Open...

The Issue: Labeling Not Elsewhere Classified: Product labeled to contain methanol

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2020· Santa Cruz Biotechnology, Inc

Recalled Item: UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol) Recalled...

The Issue: Subpotent drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2020· Natures Path Foods USA, Inc.

Recalled Item: Gluten-Free Organic Mesa Sunrise Cereal USA Recalled by Natures Path Foods...

The Issue: Undeclared Wheat and/or Barley.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 7, 2020· High Liner Foods Inc.

Recalled Item: HIGH LINER FOODSERVICE***Genuine Maryland-Style Premium Crab Cakes***48-3...

The Issue: Product contains undeclared hydrolyzed soy protein.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2020· Tosoh Bioscience Inc

Recalled Item: Tosoh Bioscience AIA-PACK BHCG Calibration Verification Test Set-In Vitro...

The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) Recalled by Maquet...

The Issue: Instruction For Use (IFU) incorrect serial number of 90437000. It should...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2020· Tosoh Bioscience Inc

Recalled Item: Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for...

The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Boston Scientific Corporation

Recalled Item: WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent)...

The Issue: Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· Inpeco S.A.

Recalled Item: FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot)...

The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2020· TELEFLEX MEDICAL INC

Recalled Item: Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is...

The Issue: Potential sterility issue

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

Class II — Potential Health HazardOngoing
FoodAugust 6, 2020· La Canasta Mexican Food Products, Inc.

Recalled Item: My Nana's Thick & Crunchy Tortilla Chips Recalled by La Canasta Mexican Food...

The Issue: Tortilla chips turn stale prior to expiration date.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 6, 2020· C-RAD POSITIONING AB

Recalled Item: PC Application Software c4D as part of the device Catalyst: Recalled by...

The Issue: PC Application Software c4D not changing Site upon synchronization during...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Carl Zeiss Meditec AG

Recalled Item: Carl Zeiss Meditec AG VISUREF150 - Product Usage: Recalled by Carl Zeiss...

The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Carl Zeiss Meditec AG

Recalled Item: Carl Zeiss Meditec Ag VISULENS 550 - Product Recalled by Carl Zeiss Meditec...

The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Life Technologies Corporation

Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...

The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Life Technologies Corporation

Recalled Item: The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19...

The Issue: COVID-19 Interpretive Software issues that may cause: 1) the risk of invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2020· Talladium Inc

Recalled Item: Talladium Luminesse Zirconia Discs Recalled by Talladium Inc Due to The...

The Issue: The linear shrinkage on the zirconia blank disc s part label is incorrect....

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

Class II — Potential Health HazardOngoing