State

Colorado product recalls

73,509 recalls have nationwide distribution and so reach Colorado. 6,947 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total: 6,947
Critical: 1,218
Severe: 1,823
Most recent: 2026-10-14

Of the 6,947 recalls naming Colorado we have scored against our rubric, 1,218 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,823 (26%) are Severe.

Which agencies issued them

These figures cover only the 6,947 recalls whose distribution notice names Colorado specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23226–23250 of 80456

HighFDA (Food)·F-0894-2022·2022-03-23
Fresh Creative Foods Couscous Kit Recalled for Plastic Contamination
Fresh Creative Foods has recalled its Autumn Couscous with Butternut Squash Kit due to hard plastic pieces found in the product from contaminated ice. No injuries have been reported.
Product
Fresh Creative Foods AUTUMN COUSCOUS W/ BUTTERNUT SQUASH KIT V 2/3.1875 LB UPC: 1001345432377 Item # 406627 Perishable/Keep refrigerated Kit Components: 2/2.75 lb. tubs of autumn couscous salad, 2/4 oz. bags of pecan cranberry blend, 1/6 oz. bags of product kit., distributed…
Category
Food
Distribution
20 states
HighNHTSA·22V175000·2022-03-23
Brake pressure switch corrosion in Arcimoto motorcycles may cause constant brake lights
Arcimoto Inc. is recalling certain 2019-2022 motorcycles because the brake pressure switch may corrode when exposed to salt and de-icer chemicals. Corroded switches cause brake lights to illuminate constantly, confusing other drivers and increasing crash risk.
Product
ARCIMOTO — ARCIMOTO FUV, RAPID RESPONDER, DELIVERATOR, ROADSTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0761-2022·2022-03-23
Boston Scientific Hydratome RX Devices Recalled Due to Sterile Barrier Breach
Boston Scientific is recalling Hydratome RX 44-30MM/260CM devices due to a sterile barrier breach that could compromise device sterility. The recall affects 3,371 units distributed worldwide.
Product
HYDRATOME RX 44-30MM/260CM Material Number: M00583050
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0768-2022·2022-03-23
Sterile Barrier Breach in JAGTOME RX Medical Devices Worldwide
Boston Scientific is recalling 4,487 JAGTOME RX medical devices worldwide due to sterility compromise from a sterile barrier breach. Users face contamination risk if devices are used.
Product
JAGTOME RX 39-20-260-025 Material Number: M00573080
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0770-2022·2022-03-23
Boston Scientific JAGTOME RX medical device recalled for sterile barrier breach
Boston Scientific has recalled 1,447 units of the JAGTOME RX 39-30-260-025 medical device due to a compromised sterile barrier that affects device sterility. The affected devices were distributed worldwide.
Product
JAGTOME RX 39-30-260-025 Material Number: M00573100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0758-2022·2022-03-23
DREAMTOME Medical Device Recalled Due to Sterile Barrier Breach
Boston Scientific is recalling 32 units of DREAMTOME endoscopic devices due to a sterile barrier breach that compromises device sterility, creating potential infection risk. No illnesses have been reported.
Product
DREAMTOME 49-30MM/450CM Material Number: M00584030
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0860-2022·2022-03-23
Herbalife Protein Bar Deluxe recalled for undeclared egg allergen
Herbalife International is recalling Herbalife NutritionProtein Bar Deluxe in Chocolate Peanut flavor nationwide due to undeclared egg allergen. The product poses a risk to consumers with egg allergies.
Product
Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut flavor. 14 bars per carton Protein-based snack for energy and nutrition 14 bars 1.23 oz (35 g) each Net wt. 17.3 oz., (490 g) SKU: 0365US Catalog Number: 0365 Formulated and Distributed by Herbalife International of…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0871-2022·2022-03-23
Honey Sriracha Seasoning Recalled for Undeclared Wheat Allergen
PS Seasoning & Spices is recalling its Honey Sriracha Snack Stick Seasoning due to undeclared wheat. The product was distributed to multiple U.S. states and Canada.
Product
796-B Honey Sriracha Snack Stick Seasoning Net Wt 5.25 lbs. (2.38kg). Part #020001965. Ingredients: Sugar, Salt, Spice, Brown Sugar, Dried Honey, Hot Sauce Powder (aged Cayenne Red Peppers, Vinegar, Salt, Garlic), Garlic Powder, Sodium Diacetate, Sodium Erythorbate…
Category
Food
Distribution
27 states
HighFDA (Devices)·Z-0789-2022·2022-03-23
SAM CHEST SEAL devices recalled due to assembly defect preventing wound seal
Sam Medical Products is recalling 2,950 packages of SAM CHEST SEAL (Model CS203-EN, Lot Y060321-09) with defective dressing containing holes that prevent creating an occlusive seal for chest wounds.
Product
SAM CHEST SEAL REF CS203-EN Combo LOT Y060321-09
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-0806-2022·2022-03-23
Syphilis Test Reagent Pack Recalled for Vaccine Interference and Manufacturing Defects
Bio-Rad's BioPlex 2200 Syphilis Test Reagent Pack is being recalled due to concerns that COVID-19 vaccines may interfere with test results, and due to manufacturing defects affecting reagent stability.
Product
BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0800-2022·2022-03-23
SAFE-T PLUS Adult Lumbar Puncture Tray recalled for manometer failure
Bard Peripheral Vascular Inc recalled 3,240 SAFE-T PLUS Adult lumbar puncture trays due to manometer failures involving leaking and defective mating connections.
Product
SAFE-T PLUS ATRAUMATIC ADULT LP TRAY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0797-2022·2022-03-23
Lumbar Puncture Tray Devices Recalled for Manometer Leaking and Mating Issues
Bard Peripheral Vascular Inc. recalls SAFE-T PLUS lumbar puncture trays due to manometer leaking and mating issues affecting device function. The FDA Class II recall covers 15,650 devices distributed nationwide and internationally.
Product
SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0750-2022·2022-03-23
Hologic Panther Fusion Extraction Reagent-X May Produce False Test Results
Hologic is recalling Panther Fusion Extraction Reagent-X kits due to failed stability specifications that may cause false negative test results. Healthcare providers should stop using affected lots.
Product
Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X Fusion Capture reagent-X 4 EA, FER-X Fusion Enhancer Reagent-X (Lithium Hydroxide Solution) 4 EA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0769-2022·2022-03-23
JAGTOME RX medical device recalled for sterile barrier breach
Boston Scientific's JAGTOME RX medical device (367 units) is being recalled worldwide due to a sterile barrier breach that compromises device sterility.
Product
JAGTOME RX 39-20-450-025 Material Number: M00573090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0775-2022·2022-03-23
Boston Scientific JAGTOME RX device recalled for sterile barrier breach
Boston Scientific has recalled 2209 units of the JAGTOME RX medical device worldwide due to compromised sterility from a sterile barrier breach. The affected units were distributed across the US and more than 40 countries.
Product
JAGTOME RX 44-30-260-035 Material Number: M00573060
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0807-2022·2022-03-23
BioPlex 2200 Syphilis Calibrator Set Recall Due to Vaccine Interference and Reagent Stability Issues
Bio-Rad Laboratories is recalling 724 BioPlex 2200 Syphilis Calibrator sets due to COVID-19 vaccine interference concerns and manufacturing problems with reagent stability. The recalled lots were distributed nationwide in the U.S. and internationally.
Product
BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0869-2022·2022-03-23
Honey BBQ seasoning recalled due to undeclared wheat allergen
PS Seasoning & Spices recalls Honey BBQ Snack seasoning (3,001 units) distributed to 28 states and Canada due to undeclared wheat. Consumers with wheat allergies should not use affected lots.
Product
Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456. 2. 685-B, Net Wt 5.25 lbs. (2.38kg). Part #020001457. Ingredients: Sugar, Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder…
Category
Food
Distribution
27 states
HighFDA (Devices)·Z-0795-2022·2022-03-23
Lumbar Puncture Tray Adult recalled due to manometer failure and leaking
Bard Peripheral Vascular Inc is recalling 8,630 lumbar puncture trays due to manometer failure causing leaking and mating issues. Devices were distributed nationwide in the U.S. plus Puerto Rico, Costa Rica, and Hong Kong.
Product
LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0892-2022·2022-03-23
Plant-Based Chicken Chipotle Pasta Salad Kit Recalled for Plastic Contamination
Fresh Creative Foods is recalling Plant Based Chicken Chipotle Pasta Salad Kit due to hard plastic pieces found in the product. The plastic contamination came from ice purchased from a supplier.
Product
Fresh Creative Foods PLANT BASED CHICKEN CHIPOTLE PASTA SALAD KIT 2/5.8125 LB UPC: 10013454381820 Item # 404996 Kit Components: 2/4.5 lb. tubs of Chipotle Pasta Salad; 2/15 oz. bags of plant based chipotle seasoned protein strips 2/5 oz. bags of shredded cheddar cheese…
Category
Food
Distribution
20 states
HighFDA (Food)·F-0893-2022·2022-03-23
Basil Pesto Bowtie Pasta Salad Kits Recalled for Hard Plastic Contamination
Fresh Creative Foods is recalling Basil Pesto Bowtie Pasta Salad Kits because hard clear plastic pieces were found in the product during manufacturing. The plastic originated from ice purchased from the manufacturer's supplier.
Product
Fresh Creative Foods; BASIL PESTO BOWTIE PASTA SALAD DIRECT KIT 2/5.15625 LB UPC: 10013454380922; Item # 404736 Perishable/ Keep Refrigerated Kit components: 2/3 lb. bags of Bowtie Pasta, 2/24 oz. bags of Sweet Basil Dressing, 2/8 oz. bags of diced sundried tomato, 2/2.5 bags…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-0791-2022·2022-03-23
Lumbar Puncture Tray Pediatric Recalled Due to Manometer Failure
Bard Peripheral Vascular Inc is recalling pediatric lumbar puncture trays due to manometer leaking and mating failures that could prevent proper pressure measurement during procedures.
Product
LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0868-2022·2022-03-23
Rosarita Organic Refried Beans recalled for small rocks contamination
ConAgra Foods is recalling Rosarita Organic Refried Beans due to possible contamination with small rocks. The recall affects approximately 169,680 cases distributed across seven states.
Product
Rosarita Organic Refried Beans Multipack carton containing 8 - 16oz cans
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-0781-2022·2022-03-23
Boston Scientific RX Cholangiogram Kit Recall Due to Sterile Barrier Breach
Boston Scientific is recalling RX Cholangiogram Kits because the sterile barrier has been breached, compromising the sterility of the devices. The affected kits were distributed worldwide.
Product
RX CHOLANGIOGRAM KIT - SINGLE Material Number: M00575240 M00575240 M00575280 M00575320 M00575360 M00575380 M00575400 M00575440 M00575480
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0766-2022·2022-03-23
Boston Scientific recalls 68 medical devices with sterility breach
Boston Scientific is recalling 68 JAGTOME REVOLUTION RX medical devices due to sterile barrier breach. The devices were distributed worldwide including throughout the US.
Product
JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0762-2022·2022-03-23
HYDRATOME RX surgical device recalled due to sterile barrier breach
Boston Scientific recalls 251 HYDRATOME RX 44-30MM/450CM units worldwide due to sterile barrier breach that compromises device sterility.
Product
HYDRATOME RX 44-30MM/450CM Material Number: M00583070
Category
Medical Device
Distribution
Distributed nationwide