State

Colorado product recalls

73,376 recalls have nationwide distribution and so reach Colorado. 6,945 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total: 6,945
Critical: 1,218
Severe: 1,823
Most recent: 2026-10-02

Of the 6,945 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 6,945 recalls whose distribution notice names Colorado specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18201–18225 of 80321

HighFDA (Drugs)·D-0469-2023·2023-03-22
Eye allergy medication recalled for out-of-specification impurity
Teva Pharmaceuticals is recalling 715,632 bottles of Clear Eyes Once Daily eye drops due to an out-of-specification impurity found during stability testing.
Product
Clear Eyes, Once Daily, Eye Allergy Itch Relief, olopatadine hydrochloride ophthalmic solution, USP, 0.2%, Antihistamine, 2.5 mL (0.085 fl oz) bottle, Sterile, Distributed by Medtech Products Inc. Tarrytown, NY 10591, A Prestige Consumer Healthcare company, Made in Israel, UPC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1243-2023·2023-03-22
BD Ultra-Fine Insulin Syringes Recalled Due to Nonsterile Condition
Becton Dickinson is recalling BD Ultra-Fine Insulin Syringes (Catalog Number 326719) due to a nonsterile condition that could expose patients to pathogenic microorganisms and local infection. Approximately 80,500 units distributed worldwide are affected.
Product
BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326719
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1245-2023·2023-03-22
Fusion Bioline Vascular Graft recalled due to manufacturing straightness defect
Maquet Cardiovascular is recalling one Fusion Bioline Vascular Graft from lot 25162546 that failed straightness testing. The graft could reduce blood flow or cause tension, potentially leading to bleeding and pseudo-aneurysm.
Product
Fusion Bioline Vascular Graft, Part number M00201503046B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0435-2023·2023-03-22
White Confectionery Chocolate Drop May Contain Undeclared Peanut Residue
Clasen Quality Chocolater is recalling 4M White Confectionery Drop MB chocolate because it may contain undeclared peanut residue. Peanut allergen poses a risk to consumers with peanut allergies.
Product
4M White Confectionery Drop MB, Item # 56464. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Palm Kernel Oil, Nonfat Dry Milk, Whole Milk Powder, Whey Powder (Milk) Palm Oil, Sunflower Lecithin (an emulsifier), Vanilla Extract. Distributed By: Clasen…
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-1258-2023·2023-03-22
Dimension Tacrolimus Diagnostic Cartridge Recalled for Measurement Imprecision
Siemens is recalling Dimension Tacrolimus diagnostic test cartridges (lots GA2286, GA3047, GA3171) due to confirmed measurement imprecision that could lead to incorrect drug dosing and potential organ failure or toxicity.
Product
Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test for the quantitative measurement of tacrolimus in human whole blood on the Dimension¿ clinical chemistry system SMN: 10700795 (DF207)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0429-2023·2023-03-22
Milk Chocolate Wafers Recalled for Undeclared Peanut Residue
Clasen Quality Chocolate is recalling milk chocolate confectionery wafers due to potential undeclared peanut residue. Consumers with peanut allergies should not consume this product.
Product
Milk Choc Flvd Confectionery Wafer (HP, NSA), Item # 52546. Net Wt. 40 lbs. (18.14 KG) poly-lined case. Ingredients: Palm Kernal Oil, Whey Protein Isolate, Erythritol, Sodium Caseinate, Cocoa Powder (Processed with Alkali), Natural Flavor, Sunflower Lecithin (an emulsifier)…
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-1257-2023·2023-03-22
Beckman Coulter Access Immunoassay Analyzers Recalled for Defective Nut Bands
Beckman Coulter is recalling approximately 4,100 laboratory immunoassay analyzers due to defective nut bands that may cause operational failures and erroneous patient test results.
Product
Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N); (2) Access 2 Immunoassay Analyzer, Refurbished (386220); (3) Access 2 Immunoassay Analyzer, Refurbished (A65531) ; and (4) Access 2 Section, DxC 600i Packaged(A25640).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1237-2023·2023-03-22
BD Ultra-Fine Insulin Syringe Recall Due to Nonsterile Manufacturing
Becton Dickinson is recalling 45,000 units of BD Ultra-Fine Insulin Syringes (catalog 326679, lot 2164338) due to nonsterile manufacturing that could expose patients to pathogenic microorganisms and local infection. Distribution was worldwide.
Product
BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326679
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0621-2023·2023-03-22
Frozen Wonton Wrappers Recalled Due to Peanut Contamination in Sub-Ingredient
Bailey International Foods is recalling 4" x 4" and 3.5" x 3.5" frozen wonton wrappers due to peanut contamination in a sub-ingredient. The product was distributed to wholesalers in 19 states.
Product
Wonton wrappers, 4" x 4" and 3.5" x 3.5", packaged in 30lb. corrugated (cardboard) boxes. Product is sold frozen.
Category
Food
Distribution
19 states
HighFDA (Devices)·Z-1248-2023·2023-03-22
TFN Femoral Nails dimensions mislabeled, may measure 170mm or 200mm
Synthes recalled TFN-Advanced Femoral Nails because some units have incorrect dimensions: nails labeled 200mm may measure 170mm, while those labeled 170mm may measure 200mm. This dimensional mismatch could compromise surgical fixation.
Product
TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Intended for temporary fixation and stabilization of proximal femur fractures Part Number: 04.037.242S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0438-2023·2023-03-22
Chocolate Baking Chips Recalled Due to Undeclared Peanut Residue
Clasen Quality Chocolater has recalled 4M DF NSA Semisweet Baking Drop chocolate due to potential undeclared peanut residue. The product may pose a risk to consumers with peanut allergies.
Product
4M DF NSA Semisweet Baking Drop (FT), Item # 56854. Net Wt. 40 lbs. (18.14 KG) poly-lined case. Ingredients: Chocolate Liquor, Inulin, Erythritol, Cocoa Butter, Sunflower Lecithin (an emulsifier), Vanilla Extract, Stevia Leaf Reb M. Distributed By: Clasen Quality…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0618-2023·2023-03-22
Spicy Kick snack mix recalled due to potential metal contamination
Catalina Snacks is recalling Spicy Kick ready-to-eat snack mix pouches due to potential metal contamination. The product was distributed across multiple U.S. states and online sales.
Product
Spicy Kick flavored ready-to-eat snack mix packaged in 6oz (UPC 850017468153) plastic stand up pouch.
Category
Food
Distribution
21 states
HighFDA (Food)·F-0437-2023·2023-03-22
Dark Chocolate Wafer Recalled for Undeclared Peanut Residue
Clasen Quality Chocolater is recalling DF Dark Choc Flvd Wafer (Item #56810) in 50-pound cases because the product may contain undeclared peanut residue. Consumers with peanut allergies should not consume this product.
Product
DF Dark Choc Flvd Wafer (MB), Item # 56810. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Palm Kernel Oil, Cocoa Powder (processed with Alkali), Sunflower Lecithin (an emulsifier), Salt. Distributed By: Clasen Quality Chocolate, 5126 West Terrace Drive…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0428-2023·2023-03-22
White Confectionery Coating Wafer Recalled for Undeclared Peanut Residue
Clasen Quality Chocolater is recalling 20,360 lbs of white confectionery coating wafer due to possible undeclared peanut residue that poses a risk to consumers with peanut allergies.
Product
White Confectionery Coating Wafer (HP, NSA), Item # 52544. Net Wt. 40 lbs. (18.14 KG) poly-lined case. Ingredients: Palm Kernal Oil, Whey Protein Isolate, Erythritol, Sodium Caseinate, Sunflower Lecithin (an emulsifier), Salt, and Sucralose. Distributed By: Clasen Quality…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0583-2023·2023-03-22
Celestial Seasonings Mandarin Orange Spice Tea Contains Undeclared Caffeine
Celestial Seasonings Mandarin Orange Spice herbal tea K-cups contain undeclared caffeine from black tea. The recall affects 1,844 units distributed nationwide.
Product
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
Category
Food
Distribution
42 states
HighFDA (Devices)·Z-1249-2023·2023-03-22
Plato 17 Microcatheter Recalled Due to Loose Particle Risk
Scientia Vascular is recalling Plato 17 Microcatheters due to manufacturing defects that may introduce loose particles into the catheter lumen, potentially causing blood vessel blockage or inflammatory reactions.
Product
Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1255-2023·2023-03-22
Medical Device Apheresis Kit Recalled Due to Stress Leak Risk
Fenwal Inc is recalling 6,564 units in certain lots of Amicus apheresis kits because centrifuge packs may develop a stress leak. No illnesses or injuries have been reported.
Product
Amicus Exchange Kit Therapeutics. Component of Amicus Separator multiprocedural apheresis platform
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1250-2023·2023-03-22
Arial mobile application recalled for Android loading failures
Securitas Healthcare is recalling the Arial mobile application for Android devices because the app does not load or function properly. Users should stop using the app immediately.
Product
Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency and Nurse Call system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0613-2023·2023-03-22
Chocolate Peanut Butter cereal recalled due to metal contamination
Catalina Snacks is recalling Chocolate Peanut Butter cereal (9oz pouches) due to metal contamination. The recall affects approximately 316,980 pouches distributed across multiple states and online retailers.
Product
Chocolate Peanut Butter flavored ready-to-eat cereal packaged in 9oz (UPC 850017468184) plastic stand up pouch.
Category
Food
Distribution
21 states
HighFDA (Food)·F-0436-2023·2023-03-22
Chocolate Confectionery Drops Recalled Due to Undeclared Peanut Residue
Clasen Quality Chocolater is recalling 4M Cinnamon Flvd Confectionery Drops because the chocolate may contain undeclared peanut residue. Consumers with peanut allergies should not consume this product.
Product
4M Cinnamon Flvd Confectionery Drop (MB), Item # 56466. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Palm Kernel Oil, Nonfat Dry Milk, Ground Cinnamon, Sunflower Lecithin (an emulsifier). Distributed By: Clasen Quality Chocolate, 5126 West Terrace…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0432-2023·2023-03-22
Clasen Semisweet Chocolate Drops Recalled for Undeclared Peanut
Clasen Quality Chocolate recalled 2M Semisweet Chocolate Drops due to undeclared peanut residue. Approximately 150,600 lbs distributed across 12 states.
Product
2M Semisweet Chocolate Drop, Item # 53700. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Unsweetened Chocolate, Sugar, Cocoa Butter, Dextrose, Sunflower Lecithin (an emulsifier), and Vanilla Extract. Distributed By: Clasen Quality Chocolate, 5126 West Terrace…
Category
Food
Distribution
12 states
HighFDA (Drugs)·D-0463-2023·2023-03-22
Clobazam Tablets Recalled Due to Cross Contamination Risk
Breckenridge Pharmaceutical is recalling Clobazam 20 mg tablets (Lot #5210147, exp. 12/2023) nationwide due to potential cross contamination from manufacturing deviations.
Product
Clobazam Tablets, 20 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals Pvt. Ltd., Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037, NDC 51991-901-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0615-2023·2023-03-22
Maple Waffle Cereal Recalled Due to Metal Contamination
Catalina Snacks is recalling Maple Waffle flavored ready-to-eat cereal due to the potential presence of metal fragments. Consumers should not consume the affected product.
Product
Maple Waffle flavored ready-to-eat cereal packaged in 9oz (UPC 860479001539) plastic stand up pouch.
Category
Food
Distribution
21 states
HighNHTSA·23V188000·2023-03-22
Volvo Recalls 2023 Models for False Emergency Call System Warnings
Volvo is recalling 2023 S60, C40, XC40, V60CC, XC60, and XC90 vehicles because a false warning may mask an actual emergency call system failure.
Product
VOLVO — VOLVO S60, C40BEV, XC40, V60CC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1262-2023·2023-03-22
da Vinci Surgical System Patient Cart Ballscrew Failure Risk
Intuitive Surgical recalls Patient Side Carts for da Vinci X and Xi surgical systems due to ballscrew failure risk. The failure could cause uncontrolled carriage movement leading to potential tissue injury during surgery. 9 units affected.
Product
Patient Side Cart, REF: 380620, with instrument arms, used as part of the da Vinci X Surgical System, REF: IS4200; Patient Side Cart, REF: 380652, with instrument arms, used as part of the da Vinci Xi Surgical System, REF: IS4000
Category
Medical Device
Distribution
Distributed nationwide