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. 2,489 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,489 in last 12 months

Showing 3408134100 of 51,434 recalls

Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch Recalled...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-000VF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T100-022WF Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker AutoPlex System. Model Numbers 0607-687-000 Recalled by Stryker...

The Issue: The Piston Head can become separated from the Delivery Piston, blocking the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T105-000WC IV Set w/2 Y-Sites Recalled by WalkMed Infusion, LLC Due to...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T095-022 Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2016· WalkMed Infusion, LLC

Recalled Item: T090-000 90" 20 Drop IV Admin Set. Packaged in a Tyvek pouch Recalled by...

The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2016· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire Recalled by Cardiovascular Systems...

The Issue: The pouch label was missing the use by date (UBD) of 2018-04.

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

Class II — Potential Health HazardOngoing
FoodJune 13, 2016· National Frozen Foods Corporation

Recalled Item: Not Ready to Eat Recalled by National Frozen Foods Corporation Due to...

The Issue: Not Ready To Eat IQF Peas and Carrots are recalled because they have a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· National Frozen Foods Corporation

Recalled Item: Not Ready to Eat Recalled by National Frozen Foods Corporation Due to...

The Issue: Not Ready To Eat IQF Mixed Vegetables are recalled because they have a...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Keebler 5 Flavor Mod Recalled by Kellogg Company Due to Undeclared Allergen

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Keebler Animals Crackers Recalled by Kellogg Company Due to Undeclared Allergen

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Kellogg's Special K Mini Brownies Fudge Recalled by Kellogg Company Due to...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Kellogg's Special K Mini Brownies Blondie Recalled by Kellogg Company Due to...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Gripz Variety On the Go Pack Recalled by Kellogg Company Due to Undeclared...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Keebler Animal Totes Recalled by Kellogg Company Due to Undeclared Allergen

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 13, 2016· Kellogg Company

Recalled Item: Famous Amos Cookies Chocolate Chip Recalled by Kellogg Company Due to...

The Issue: Kellogg Company initiated a voluntary recall of multiple snack food items...

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

Class II — Potential Health HazardOngoing
Refund