Colorado Recalls

5,033 recalls on record affecting Colorado

medical Class II
2026-07-22

Orthofix U.S. LLC recalls Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

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medical Class II
2026-07-22

Orthofix U.S. LLC recalls Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF:

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

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medical Class II
2026-07-22

Orthofix U.S. LLC recalls Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF:

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

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medical Class II
2026-07-22

Orthofix U.S. LLC recalls Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

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Food Class II
2026-07-22

AMY'S KITCHEN INC. recalls Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ

Potential for spoilage.

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Food Class II
2026-07-22

Nutricia North America recalls functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPL

Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

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Food Class II
2026-07-22

Nutricia North America recalls functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL

Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

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medical Class II
2026-07-15

Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS,

Due to packaging discrepancy with incorrect product size mixed up.

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medical Class II
2026-07-15

Encore Medical, LP recalls Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS,

Due to packaging discrepancy with incorrect product size mixed up.

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medical Class II
2026-07-08

Medela Inc recalls Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml

May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritional fluids or oral medication.

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Food Class II
2026-07-08

MARS SNACKING recalls MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Pr

Potential contamination with plastic material

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Food Class II
2026-07-08

MARS SNACKING recalls MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein

Potential contamination with plastic material

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drugs Class II
2026-07-01

PReye LLC recalls PReye Vitamin See Antioxidant Preservative Free Eye Drops, D

Lack of Assurance of Sterility

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Food Class I
2026-07-01

Utz Quality Foods, LLC recalls 2.5oz , 8oz , Zapp's Brand Bayou Blackened Ranch Potato Chi

Potential presence of Salmonella.

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Food Class I
2026-07-01

Utz Quality Foods, LLC recalls 1.5oz, 8.0oz , Zapp's Big Cheezy Potato Chips, Plastic Bag.

Potential presence of Salmonella.

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Food Class I
2026-07-01

Utz Quality Foods, LLC recalls 2.0 oz Dirty Maui Onion Chip, Plastic Bag.

Potential presence of Salmonella.

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Food Class I
2026-07-01

Utz Quality Foods, LLC recalls 1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag

Potential presence of Salmonella.

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Food Class I
2026-07-01

Utz Quality Foods, LLC recalls 2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.

Potential presence of Salmonella.

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Food Class I
2026-07-01

Utz Quality Foods, LLC recalls 1.5oz, 2oz Dirty Brand Salt and Vinegar Potato Chips , Plast

Potential presence of Salmonella.

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medical Class II
2026-06-24

Beta Bionics, Inc. recalls iLet Bionic Pancreas, REF: BB1001

The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the user successfully slides the unlock slider on the Lock Screen, no screen transition occurs, and the user remains on the Lock Screen. Because the user cannot exit the Lock Screen, the user is unable to perform a cartridge change or meal announcement. If this occurs and therapy is in progress, therapy will continue normally until the insulin cartridge is depleted. The user will be unable to perform a cartridge change or a meal announcement and will be stuck on the screen until the battery fully drains. This can lead to hyperglycemia.

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Showing 20 of 5,033 recalls. Use search to filter further.